Illinois 2023-2024 Regular Session

Illinois House Bill HB4637 Latest Draft

Bill / Introduced Version Filed 01/30/2024

                            103RD GENERAL ASSEMBLY State of Illinois 2023 and 2024 HB4637 Introduced , by Rep. Fred Crespo SYNOPSIS AS INTRODUCED: 225 ILCS 95/4 from Ch. 111, par. 4604225 ILCS 95/6 from Ch. 111, par. 4606225 ILCS 95/7 from Ch. 111, par. 4607225 ILCS 95/7.5225 ILCS 95/7.7225 ILCS 95/7.8 new225 ILCS 95/7.9 new225 ILCS 95/17 from Ch. 111, par. 4617225 ILCS 95/20 from Ch. 111, par. 4620225 ILCS 95/21 from Ch. 111, par. 4621720 ILCS 570/102 from Ch. 56 1/2, par. 1102720 ILCS 570/303.05 Amends the Physician Assistant Practice Act of 1987. Provides that a physician assistant may prescribe, dispense, order, administer, and procure drugs and medical devices without delegation of authority by a physician. Provides that a physician assistant may practice without a written collaborative agreement. Provides that a physician assistant who files with the Department of Financial and Professional Regulation a notarized attestation of completion of at least 250 hours of continuing education or training and at least 2,000 hours of clinical experience after first attaining national certification shall not require a written collaborative agreement. Makes changes in provisions concerning definitions; physician assistant title; collaboration requirements; written collaborative agreements, prescriptive authority, and physician assistants in hospitals, hospital affiliates, or ambulatory surgical treatment centers; inactive status; limitations; and grounds for disciplinary action. Amends the Illinois Controlled Substances Act to make corresponding changes. LRB103 35424 SPS 65490 b   A BILL FOR 103RD GENERAL ASSEMBLY State of Illinois 2023 and 2024 HB4637 Introduced , by Rep. Fred Crespo SYNOPSIS AS INTRODUCED:  225 ILCS 95/4 from Ch. 111, par. 4604225 ILCS 95/6 from Ch. 111, par. 4606225 ILCS 95/7 from Ch. 111, par. 4607225 ILCS 95/7.5225 ILCS 95/7.7225 ILCS 95/7.8 new225 ILCS 95/7.9 new225 ILCS 95/17 from Ch. 111, par. 4617225 ILCS 95/20 from Ch. 111, par. 4620225 ILCS 95/21 from Ch. 111, par. 4621720 ILCS 570/102 from Ch. 56 1/2, par. 1102720 ILCS 570/303.05 225 ILCS 95/4 from Ch. 111, par. 4604 225 ILCS 95/6 from Ch. 111, par. 4606 225 ILCS 95/7 from Ch. 111, par. 4607 225 ILCS 95/7.5  225 ILCS 95/7.7  225 ILCS 95/7.8 new  225 ILCS 95/7.9 new  225 ILCS 95/17 from Ch. 111, par. 4617 225 ILCS 95/20 from Ch. 111, par. 4620 225 ILCS 95/21 from Ch. 111, par. 4621 720 ILCS 570/102 from Ch. 56 1/2, par. 1102 720 ILCS 570/303.05  Amends the Physician Assistant Practice Act of 1987. Provides that a physician assistant may prescribe, dispense, order, administer, and procure drugs and medical devices without delegation of authority by a physician. Provides that a physician assistant may practice without a written collaborative agreement. Provides that a physician assistant who files with the Department of Financial and Professional Regulation a notarized attestation of completion of at least 250 hours of continuing education or training and at least 2,000 hours of clinical experience after first attaining national certification shall not require a written collaborative agreement. Makes changes in provisions concerning definitions; physician assistant title; collaboration requirements; written collaborative agreements, prescriptive authority, and physician assistants in hospitals, hospital affiliates, or ambulatory surgical treatment centers; inactive status; limitations; and grounds for disciplinary action. Amends the Illinois Controlled Substances Act to make corresponding changes.  LRB103 35424 SPS 65490 b     LRB103 35424 SPS 65490 b   A BILL FOR
103RD GENERAL ASSEMBLY State of Illinois 2023 and 2024 HB4637 Introduced , by Rep. Fred Crespo SYNOPSIS AS INTRODUCED:
225 ILCS 95/4 from Ch. 111, par. 4604225 ILCS 95/6 from Ch. 111, par. 4606225 ILCS 95/7 from Ch. 111, par. 4607225 ILCS 95/7.5225 ILCS 95/7.7225 ILCS 95/7.8 new225 ILCS 95/7.9 new225 ILCS 95/17 from Ch. 111, par. 4617225 ILCS 95/20 from Ch. 111, par. 4620225 ILCS 95/21 from Ch. 111, par. 4621720 ILCS 570/102 from Ch. 56 1/2, par. 1102720 ILCS 570/303.05 225 ILCS 95/4 from Ch. 111, par. 4604 225 ILCS 95/6 from Ch. 111, par. 4606 225 ILCS 95/7 from Ch. 111, par. 4607 225 ILCS 95/7.5  225 ILCS 95/7.7  225 ILCS 95/7.8 new  225 ILCS 95/7.9 new  225 ILCS 95/17 from Ch. 111, par. 4617 225 ILCS 95/20 from Ch. 111, par. 4620 225 ILCS 95/21 from Ch. 111, par. 4621 720 ILCS 570/102 from Ch. 56 1/2, par. 1102 720 ILCS 570/303.05
225 ILCS 95/4 from Ch. 111, par. 4604
225 ILCS 95/6 from Ch. 111, par. 4606
225 ILCS 95/7 from Ch. 111, par. 4607
225 ILCS 95/7.5
225 ILCS 95/7.7
225 ILCS 95/7.8 new
225 ILCS 95/7.9 new
225 ILCS 95/17 from Ch. 111, par. 4617
225 ILCS 95/20 from Ch. 111, par. 4620
225 ILCS 95/21 from Ch. 111, par. 4621
720 ILCS 570/102 from Ch. 56 1/2, par. 1102
720 ILCS 570/303.05
Amends the Physician Assistant Practice Act of 1987. Provides that a physician assistant may prescribe, dispense, order, administer, and procure drugs and medical devices without delegation of authority by a physician. Provides that a physician assistant may practice without a written collaborative agreement. Provides that a physician assistant who files with the Department of Financial and Professional Regulation a notarized attestation of completion of at least 250 hours of continuing education or training and at least 2,000 hours of clinical experience after first attaining national certification shall not require a written collaborative agreement. Makes changes in provisions concerning definitions; physician assistant title; collaboration requirements; written collaborative agreements, prescriptive authority, and physician assistants in hospitals, hospital affiliates, or ambulatory surgical treatment centers; inactive status; limitations; and grounds for disciplinary action. Amends the Illinois Controlled Substances Act to make corresponding changes.
LRB103 35424 SPS 65490 b     LRB103 35424 SPS 65490 b
    LRB103 35424 SPS 65490 b
A BILL FOR
HB4637LRB103 35424 SPS 65490 b   HB4637  LRB103 35424 SPS 65490 b
  HB4637  LRB103 35424 SPS 65490 b
1  AN ACT concerning regulation.
2  Be it enacted by the People of the State of Illinois,
3  represented in the General Assembly:
4  Section 5. The Physician Assistant Practice Act of 1987 is
5  amended by changing Sections 4, 6, 7, 7.5, 7.7, 17, 20, and 21
6  and by adding Sections 7.8 and 7.9 as follows:
7  (225 ILCS 95/4) (from Ch. 111, par. 4604)
8  (Text of Section before amendment by P.A. 103-65)
9  (Section scheduled to be repealed on January 1, 2028)
10  Sec. 4. Definitions. In this Act:
11  1. "Department" means the Department of Financial and
12  Professional Regulation.
13  2. "Secretary" means the Secretary of Financial and
14  Professional Regulation.
15  3. "Physician assistant" means any person not holding an
16  active license or permit issued by the Department pursuant to
17  the Medical Practice Act of 1987 who has been certified as a
18  physician assistant by the National Commission on the
19  Certification of Physician Assistants or equivalent successor
20  agency and performs procedures in collaboration with a
21  physician as defined in this Act. A physician assistant may
22  perform such procedures within the specialty of the
23  collaborating physician, except that such physician shall

 

103RD GENERAL ASSEMBLY State of Illinois 2023 and 2024 HB4637 Introduced , by Rep. Fred Crespo SYNOPSIS AS INTRODUCED:
225 ILCS 95/4 from Ch. 111, par. 4604225 ILCS 95/6 from Ch. 111, par. 4606225 ILCS 95/7 from Ch. 111, par. 4607225 ILCS 95/7.5225 ILCS 95/7.7225 ILCS 95/7.8 new225 ILCS 95/7.9 new225 ILCS 95/17 from Ch. 111, par. 4617225 ILCS 95/20 from Ch. 111, par. 4620225 ILCS 95/21 from Ch. 111, par. 4621720 ILCS 570/102 from Ch. 56 1/2, par. 1102720 ILCS 570/303.05 225 ILCS 95/4 from Ch. 111, par. 4604 225 ILCS 95/6 from Ch. 111, par. 4606 225 ILCS 95/7 from Ch. 111, par. 4607 225 ILCS 95/7.5  225 ILCS 95/7.7  225 ILCS 95/7.8 new  225 ILCS 95/7.9 new  225 ILCS 95/17 from Ch. 111, par. 4617 225 ILCS 95/20 from Ch. 111, par. 4620 225 ILCS 95/21 from Ch. 111, par. 4621 720 ILCS 570/102 from Ch. 56 1/2, par. 1102 720 ILCS 570/303.05
225 ILCS 95/4 from Ch. 111, par. 4604
225 ILCS 95/6 from Ch. 111, par. 4606
225 ILCS 95/7 from Ch. 111, par. 4607
225 ILCS 95/7.5
225 ILCS 95/7.7
225 ILCS 95/7.8 new
225 ILCS 95/7.9 new
225 ILCS 95/17 from Ch. 111, par. 4617
225 ILCS 95/20 from Ch. 111, par. 4620
225 ILCS 95/21 from Ch. 111, par. 4621
720 ILCS 570/102 from Ch. 56 1/2, par. 1102
720 ILCS 570/303.05
Amends the Physician Assistant Practice Act of 1987. Provides that a physician assistant may prescribe, dispense, order, administer, and procure drugs and medical devices without delegation of authority by a physician. Provides that a physician assistant may practice without a written collaborative agreement. Provides that a physician assistant who files with the Department of Financial and Professional Regulation a notarized attestation of completion of at least 250 hours of continuing education or training and at least 2,000 hours of clinical experience after first attaining national certification shall not require a written collaborative agreement. Makes changes in provisions concerning definitions; physician assistant title; collaboration requirements; written collaborative agreements, prescriptive authority, and physician assistants in hospitals, hospital affiliates, or ambulatory surgical treatment centers; inactive status; limitations; and grounds for disciplinary action. Amends the Illinois Controlled Substances Act to make corresponding changes.
LRB103 35424 SPS 65490 b     LRB103 35424 SPS 65490 b
    LRB103 35424 SPS 65490 b
A BILL FOR

 

 

225 ILCS 95/4 from Ch. 111, par. 4604
225 ILCS 95/6 from Ch. 111, par. 4606
225 ILCS 95/7 from Ch. 111, par. 4607
225 ILCS 95/7.5
225 ILCS 95/7.7
225 ILCS 95/7.8 new
225 ILCS 95/7.9 new
225 ILCS 95/17 from Ch. 111, par. 4617
225 ILCS 95/20 from Ch. 111, par. 4620
225 ILCS 95/21 from Ch. 111, par. 4621
720 ILCS 570/102 from Ch. 56 1/2, par. 1102
720 ILCS 570/303.05



    LRB103 35424 SPS 65490 b

 

 



 

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1  exercise such direction, collaboration, and control over such
2  physician assistants as will assure that patients shall
3  receive quality medical care. Physician assistants shall be
4  capable of performing a variety of tasks within the specialty
5  of medical care in collaboration with a physician.
6  Collaboration with the physician assistant shall not be
7  construed to necessarily require the personal presence of the
8  collaborating physician at all times at the place where
9  services are rendered, as long as there is communication
10  available for consultation by radio, telephone or
11  telecommunications within established guidelines as determined
12  by the physician/physician assistant team. The collaborating
13  physician may delegate tasks and duties to the physician
14  assistant. Delegated tasks or duties shall be consistent with
15  physician assistant education, training, and experience. The
16  delegated tasks or duties shall be specific to the practice
17  setting and shall be implemented and reviewed under a written
18  collaborative agreement established by the physician or
19  physician/physician assistant team. A physician assistant,
20  acting as an agent of the physician, shall be permitted to
21  transmit the collaborating physician's orders as determined by
22  the institution's bylaws by-laws, policies, procedures, or job
23  description within which the physician/physician assistant
24  team practices. Physician assistants shall practice only in
25  accordance with a written collaborative agreement.
26  Any person who holds an active license or permit issued

 

 

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1  pursuant to the Medical Practice Act of 1987 shall have that
2  license automatically placed into inactive status upon
3  issuance of a physician assistant license. Any person who
4  holds an active license as a physician assistant who is issued
5  a license or permit pursuant to the Medical Practice Act of
6  1987 shall have his or her physician assistant license
7  automatically placed into inactive status.
8  3.5. "Physician assistant practice" means the performance
9  of procedures within the specialty of the collaborating
10  physician. Physician assistants shall be capable of performing
11  a variety of tasks within the specialty of medical care of the
12  collaborating physician. Collaboration with the physician
13  assistant shall not be construed to necessarily require the
14  personal presence of the collaborating physician at all times
15  at the place where services are rendered, as long as there is
16  communication available for consultation by radio, telephone,
17  telecommunications, or electronic communications. The
18  collaborating physician may delegate tasks and duties to the
19  physician assistant. Delegated tasks or duties shall be
20  consistent with physician assistant education, training, and
21  experience. The delegated tasks or duties shall be specific to
22  the practice setting and shall be implemented and reviewed
23  under a written collaborative agreement established by the
24  physician or physician/physician assistant team. A physician
25  assistant shall be permitted to transmit the collaborating
26  physician's orders as determined by the institution's bylaws,

 

 

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1  policies, or procedures or the job description within which
2  the physician/physician assistant team practices. Physician
3  assistants shall practice only in accordance with a written
4  collaborative agreement, except as provided in Section 7.5 of
5  this Act.
6  4. "Board" means the Medical Licensing Board constituted
7  under the Medical Practice Act of 1987.
8  5. (Blank).
9  6. "Physician" means a person licensed to practice
10  medicine in all of its branches under the Medical Practice Act
11  of 1987.
12  7. "Collaborating physician" means the physician who,
13  within his or her specialty and expertise, may delegate a
14  variety of tasks and procedures to the physician assistant.
15  Such tasks and procedures shall be delegated in accordance
16  with a written collaborative agreement.
17  8. (Blank).
18  9. "Address of record" means the designated address
19  recorded by the Department in the applicant's or licensee's
20  application file or license file maintained by the
21  Department's licensure maintenance unit.
22  10. "Hospital affiliate" means a corporation, partnership,
23  joint venture, limited liability company, or similar
24  organization, other than a hospital, that is devoted primarily
25  to the provision, management, or support of health care
26  services and that directly or indirectly controls, is

 

 

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1  controlled by, or is under common control of the hospital. For
2  the purposes of this definition, "control" means having at
3  least an equal or a majority ownership or membership interest.
4  A hospital affiliate shall be 100% owned or controlled by any
5  combination of hospitals, their parent corporations, or
6  physicians licensed to practice medicine in all its branches
7  in Illinois. "Hospital affiliate" does not include a health
8  maintenance organization regulated under the Health
9  Maintenance Organization Act.
10  11. "Email address of record" means the designated email
11  address recorded by the Department in the applicant's
12  application file or the licensee's license file, as maintained
13  by the Department's licensure maintenance unit.
14  (Source: P.A. 102-1117, eff. 1-13-23.)
15  (Text of Section after amendment by P.A. 103-65)
16  (Section scheduled to be repealed on January 1, 2028)
17  Sec. 4. Definitions. In this Act:
18  1. "Department" means the Department of Financial and
19  Professional Regulation.
20  2. "Secretary" means the Secretary of Financial and
21  Professional Regulation.
22  3. "Physician assistant" means any person not holding an
23  active license or permit issued by the Department pursuant to
24  the Medical Practice Act of 1987 who has been certified as a
25  physician assistant by the National Commission on the

 

 

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1  Certification of Physician Assistants or equivalent successor
2  agency. and performs procedures in collaboration with a
3  physician as defined in this Act. A physician assistant may
4  perform such procedures within the specialty of the
5  collaborating physician, except that such physician shall
6  exercise such direction, collaboration, and control over such
7  physician assistants as will assure that patients shall
8  receive quality medical care. Physician assistants shall be
9  capable of performing a variety of tasks within the specialty
10  of medical care in collaboration with a physician.
11  Collaboration with the physician assistant shall not be
12  construed to necessarily require the personal presence of the
13  collaborating physician at all times at the place where
14  services are rendered, as long as there is communication
15  available for consultation by radio, telephone or
16  telecommunications within established guidelines as determined
17  by the physician/physician assistant team. The collaborating
18  physician may delegate tasks and duties to the physician
19  assistant. Delegated tasks or duties shall be consistent with
20  physician assistant education, training, and experience. The
21  delegated tasks or duties shall be specific to the practice
22  setting and shall be implemented and reviewed under a written
23  collaborative agreement established by the physician or
24  physician/physician assistant team. A physician assistant,
25  acting as an agent of the physician, shall be permitted to
26  transmit the collaborating physician's orders as determined by

 

 

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  HB4637 - 7 - LRB103 35424 SPS 65490 b
1  the institution's by-laws, policies, procedures, or job
2  description within which the physician/physician assistant
3  team practices. Physician assistants shall practice only in
4  accordance with a written collaborative agreement.
5  Any person who holds an active license or permit issued
6  pursuant to the Medical Practice Act of 1987 shall have that
7  license automatically placed into inactive status upon
8  issuance of a physician assistant license. Any person who
9  holds an active license as a physician assistant who is issued
10  a license or permit pursuant to the Medical Practice Act of
11  1987 shall have his or her physician assistant license
12  automatically placed into inactive status.
13  3.5. "Physician assistant practice" means the performance
14  of any legal medical service for which the physician assistant
15  has been prepared by the physician assistant's education,
16  training, and experience and is competent to perform as
17  determined by the practice through employment agreement or
18  credentialing and privileging system of the licensed facility.
19  Medical and surgical services provided by physician assistants
20  include, but are not limited to:
21  (A) obtaining and performing comprehensive health
22  histories and physical examinations;
23  (B) evaluating, diagnosing, managing, and providing
24  medical treatment;
25  (C) ordering, performing, and interpreting diagnostic
26  studies and therapeutic procedures;

 

 

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1  (D) educating patients on health promotion and disease
2  prevention;
3  (E) providing consultation upon request;
4  (F) writing medical orders;
5  (G) prescribing, dispensing, ordering, administering,
6  and procuring drugs and medical devices; and
7  (H) assisting in surgery. procedures within the
8  specialty of the collaborating physician. Physician
9  assistants shall be capable of performing a variety of
10  tasks within the specialty of medical care of the
11  collaborating physician. Collaboration with the physician
12  assistant shall not be construed to necessarily require
13  the personal presence of the collaborating physician at
14  all times at the place where services are rendered, as
15  long as there is communication available for consultation
16  by radio, telephone, telecommunications, or electronic
17  communications. The collaborating physician may delegate
18  tasks and duties to the physician assistant. Delegated
19  tasks or duties shall be consistent with physician
20  assistant education, training, and experience. The
21  delegated tasks or duties shall be specific to the
22  practice setting and shall be implemented and reviewed
23  under a written collaborative agreement established by the
24  physician or physician/physician assistant team. A
25  physician assistant shall be permitted to transmit the
26  collaborating physician's orders as determined by the

 

 

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1  institution's bylaws, policies, or procedures or the job
2  description within which the physician/physician assistant
3  team practices. Physician assistants shall practice only
4  in accordance with a written collaborative agreement,
5  except as provided in Section 7.5 of this Act.
6  4. "Board" means the Illinois State Medical Board Medical
7  Licensing Board constituted under the Medical Practice Act of
8  1987.
9  5. (Blank).
10  6. "Physician" means a person licensed to practice
11  medicine in all of its branches under the Medical Practice Act
12  of 1987.
13  7. "Collaborating physician" means the physician who,
14  within his or her specialty and expertise, may delegate a
15  variety of tasks and procedures to the physician assistant.
16  Such tasks and procedures shall be delegated in accordance
17  with a written collaborative agreement when the agreement is
18  required under this Act.
19  8. (Blank).
20  9. "Address of record" means the designated address
21  recorded by the Department in the applicant's or licensee's
22  application file or license file maintained by the
23  Department's licensure maintenance unit.
24  10. "Hospital affiliate" means a corporation, partnership,
25  joint venture, limited liability company, or similar
26  organization, other than a hospital, that is devoted primarily

 

 

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1  to the provision, management, or support of health care
2  services and that directly or indirectly controls, is
3  controlled by, or is under common control of the hospital. For
4  the purposes of this definition, "control" means having at
5  least an equal or a majority ownership or membership interest.
6  A hospital affiliate shall be 100% owned or controlled by any
7  combination of hospitals, their parent corporations, or
8  physicians licensed to practice medicine in all its branches
9  in Illinois. "Hospital affiliate" does not include a health
10  maintenance organization regulated under the Health
11  Maintenance Organization Act.
12  11. "Email address of record" means the designated email
13  address recorded by the Department in the applicant's
14  application file or the licensee's license file, as maintained
15  by the Department's licensure maintenance unit.
16  12. "Federally qualified health center" means a health
17  center funded under Section 330 of the federal Public Health
18  Service Act.
19  (Source: P.A. 102-1117, eff. 1-13-23; 103-65, eff. 1-1-24.)
20  (225 ILCS 95/6) (from Ch. 111, par. 4606)
21  (Section scheduled to be repealed on January 1, 2028)
22  Sec. 6. Physician assistant title.
23  (a) No physician assistant shall use the title of doctor,
24  physician, or associate with his or her name or any other term
25  that would indicate to other persons that he or she is

 

 

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1  qualified to engage in the general practice of medicine.
2  (b) A physician assistant shall verbally identify himself
3  or herself as a physician assistant, including, when
4  applicable, specialty certification, to each patient.
5  (c) Nothing in this Act shall be construed to relieve a
6  physician assistant of the professional or legal
7  responsibility for the care and treatment of persons attended
8  by him or her.
9  (d) (Blank). The collaborating physician shall file with
10  the Department notice of employment, discharge, or
11  collaboration with a physician assistant within 60 days of
12  employment, discharge, or assumption of collaboration with a
13  physician assistant. Nothing in this Section shall prevent a
14  physician assistant from beginning his or her employment
15  before the notice of employment or collaboration has been
16  filed.
17  (Source: P.A. 102-735, eff. 1-1-23.)
18  (225 ILCS 95/7) (from Ch. 111, par. 4607)
19  (Text of Section before amendment by P.A. 103-65)
20  (Section scheduled to be repealed on January 1, 2028)
21  Sec. 7. Collaboration requirements.
22  (a) A collaborating physician shall determine the number
23  of physician assistants to collaborate with, provided the
24  physician is able to provide adequate collaboration as
25  outlined in the written collaborative agreement required under

 

 

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1  Section 7.5 of this Act and consideration is given to the
2  nature of the physician's practice, complexity of the patient
3  population, and the experience of each physician assistant. A
4  collaborating physician may collaborate with a maximum of 7
5  full-time equivalent physician assistants as described in
6  Section 54.5 of the Medical Practice Act of 1987. As used in
7  this Section, "full-time equivalent" means the equivalent of
8  40 hours per week per individual. Physicians and physician
9  assistants who work in a hospital, hospital affiliate, or
10  ambulatory surgical treatment center as defined by Section 7.7
11  of this Act are exempt from the collaborative ratio
12  restriction requirements of this Section. A physician
13  assistant shall be able to hold more than one professional
14  position. A collaborating physician shall file a notice of
15  collaboration of each physician assistant according to the
16  rules of the Department.
17  Physician assistants shall collaborate only with
18  physicians as defined in this Act who are engaged in clinical
19  practice, or in clinical practice in public health or other
20  community health facilities.
21  Nothing in this Act shall be construed to limit the
22  delegation of tasks or duties by a physician to a nurse or
23  other appropriately trained personnel.
24  Nothing in this Act shall be construed to prohibit the
25  employment of physician assistants by a hospital, nursing home
26  or other health care facility where such physician assistants

 

 

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1  function with under a collaborating physician.
2  A physician assistant may be employed by a practice group
3  or other entity employing multiple physicians at one or more
4  locations. In that case, one of the physicians practicing at a
5  location shall be designated the collaborating physician. The
6  other physicians with that practice group or other entity who
7  practice in the same general type of practice or specialty as
8  the collaborating physician may collaborate with the physician
9  assistant with respect to their patients.
10  (b) A physician assistant licensed in this State, or
11  licensed or authorized to practice in any other U.S.
12  jurisdiction or credentialed by his or her federal employer as
13  a physician assistant, who is responding to a need for medical
14  care created by an emergency or by a state or local disaster
15  may render such care that the physician assistant is able to
16  provide without collaboration as it is defined in this Section
17  or with such collaboration as is available.
18  Any physician who collaborates with a physician assistant
19  providing medical care in response to such an emergency or
20  state or local disaster shall not be required to meet the
21  requirements set forth in this Section for a collaborating
22  physician.
23  (Source: P.A. 100-453, eff. 8-25-17; 100-605, eff. 1-1-19.)
24  (Text of Section after amendment by P.A. 103-65)
25  (Section scheduled to be repealed on January 1, 2028)

 

 

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1  Sec. 7. Collaboration requirements.
2  (a) A written collaborative agreement is required for all
3  physician assistants engaged in clinical practice prior to
4  satisfying the requirements of Section 7.9, except for
5  physician assistants who practice in a hospital, hospital
6  affiliate, federally qualified health center, or ambulatory
7  surgical treatment center as provided in Section 7.7.
8  (b) (a) A collaborating physician shall determine the
9  number of physician assistants to collaborate with, provided
10  the physician is able to provide adequate collaboration as
11  outlined in the written collaborative agreement required under
12  Section 7.5 of this Act and consideration is given to the
13  nature of the physician's practice, complexity of the patient
14  population, and the experience of each physician assistant. A
15  collaborating physician may collaborate with a maximum of 7
16  full-time equivalent physician assistants as described in
17  Section 54.5 of the Medical Practice Act of 1987. As used in
18  this Section, "full-time equivalent" means the equivalent of
19  40 hours per week per individual. Physicians and physician
20  assistants who work in a hospital, hospital affiliate,
21  federally qualified health center, or ambulatory surgical
22  treatment center as defined by Section 7.7 of this Act are
23  exempt from the collaborative ratio restriction requirements
24  of this Section. A physician assistant shall be able to hold
25  more than one professional position. A collaborating physician
26  shall file a notice of collaboration of each physician

 

 

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1  assistant according to the rules of the Department.
2  (c) Physician assistants shall collaborate only with
3  physicians as defined in this Act who are engaged in clinical
4  practice, or in clinical practice in public health or other
5  community health facilities.
6  (d) Nothing in this Act shall be construed to limit the
7  delegation of tasks or duties by a physician to a nurse or
8  other appropriately trained personnel.
9  (e) Nothing in this Act shall be construed to prohibit the
10  employment of physician assistants by a hospital, nursing home
11  or other health care facility where such physician assistants
12  function with under a collaborating physician.
13  (f) A physician assistant may be employed by a practice
14  group or other entity employing multiple physicians at one or
15  more locations. In that case, one of the physicians practicing
16  at a location shall be designated the collaborating physician.
17  The other physicians with that practice group or other entity
18  who practice in the same general type of practice or specialty
19  as the collaborating physician may collaborate with the
20  physician assistant with respect to their patients.
21  (g) (b) A physician assistant licensed in this State, or
22  licensed or authorized to practice in any other U.S.
23  jurisdiction or credentialed by his or her federal employer as
24  a physician assistant, who is responding to a need for medical
25  care created by an emergency or by a state or local disaster
26  may render such care that the physician assistant is able to

 

 

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1  provide without collaboration as it is defined in this Section
2  or with such collaboration as is available.
3  (h) Any physician who collaborates with a physician
4  assistant providing medical care in response to such an
5  emergency or state or local disaster shall not be required to
6  meet the requirements set forth in this Section for a
7  collaborating physician.
8  (Source: P.A. 103-65, eff. 1-1-24.)
9  (225 ILCS 95/7.5)
10  (Text of Section before amendment by P.A. 103-65)
11  (Section scheduled to be repealed on January 1, 2028)
12  Sec. 7.5. Written collaborative agreements; prescriptive
13  authority.
14  (a) A written collaborative agreement is required for all
15  physician assistants to practice in the State, except as
16  provided in Section 7.7 of this Act.
17  (1) A written collaborative agreement shall describe
18  the working relationship of the physician assistant with
19  the collaborating physician and shall describe the
20  categories of care, treatment, or procedures to be
21  provided by the physician assistant. The written
22  collaborative agreement shall promote the exercise of
23  professional judgment by the physician assistant
24  commensurate with his or her education and experience. The
25  services to be provided by the physician assistant shall

 

 

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1  be services that the collaborating physician is authorized
2  to and generally provides to his or her patients in the
3  normal course of his or her clinical medical practice. The
4  written collaborative agreement need not describe the
5  exact steps that a physician assistant must take with
6  respect to each specific condition, disease, or symptom
7  but must specify which authorized procedures require the
8  presence of the collaborating physician as the procedures
9  are being performed. The relationship under a written
10  collaborative agreement shall not be construed to require
11  the personal presence of a physician at the place where
12  services are rendered. Methods of communication shall be
13  available for consultation with the collaborating
14  physician in person or by telecommunications or electronic
15  communications as set forth in the written collaborative
16  agreement. For the purposes of this Act, "generally
17  provides to his or her patients in the normal course of his
18  or her clinical medical practice" means services, not
19  specific tasks or duties, the collaborating physician
20  routinely provides individually or through delegation to
21  other persons so that the physician has the experience and
22  ability to collaborate and provide consultation.
23  (2) The written collaborative agreement shall be
24  adequate if a physician does each of the following:
25  (A) Participates in the joint formulation and
26  joint approval of orders or guidelines with the

 

 

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1  physician assistant and he or she periodically reviews
2  such orders and the services provided patients under
3  such orders in accordance with accepted standards of
4  medical practice and physician assistant practice.
5  (B) Provides consultation at least once a month.
6  (3) A copy of the signed, written collaborative
7  agreement must be available to the Department upon request
8  from both the physician assistant and the collaborating
9  physician.
10  (4) A physician assistant shall inform each
11  collaborating physician of all written collaborative
12  agreements he or she has signed and provide a copy of these
13  to any collaborating physician upon request.
14  (b) A collaborating physician may, but is not required to,
15  delegate prescriptive authority to a physician assistant as
16  part of a written collaborative agreement. This authority may,
17  but is not required to, include prescription of, selection of,
18  orders for, administration of, storage of, acceptance of
19  samples of, and dispensing medical devices, over-the-counter
20  over the counter medications, legend drugs, medical gases, and
21  controlled substances categorized as Schedule II through V
22  controlled substances, as defined in Article II of the
23  Illinois Controlled Substances Act, and other preparations,
24  including, but not limited to, botanical and herbal remedies.
25  The collaborating physician must have a valid, current
26  Illinois controlled substance license and federal registration

 

 

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1  with the Drug Enforcement Administration to delegate the
2  authority to prescribe controlled substances.
3  (1) To prescribe Schedule II, III, IV, or V controlled
4  substances under this Section, a physician assistant must
5  obtain a mid-level practitioner controlled substances
6  license. Medication orders issued by a physician assistant
7  shall be reviewed periodically by the collaborating
8  physician.
9  (2) The collaborating physician shall file with the
10  Department notice of delegation of prescriptive authority
11  to a physician assistant and termination of delegation,
12  specifying the authority delegated or terminated. Upon
13  receipt of this notice delegating authority to prescribe
14  controlled substances, the physician assistant shall be
15  eligible to register for a mid-level practitioner
16  controlled substances license under Section 303.05 of the
17  Illinois Controlled Substances Act. Nothing in this Act
18  shall be construed to limit the delegation of tasks or
19  duties by the collaborating physician to a nurse or other
20  appropriately trained persons in accordance with Section
21  54.2 of the Medical Practice Act of 1987.
22  (3) In addition to the requirements of this subsection
23  (b), a collaborating physician may, but is not required
24  to, delegate authority to a physician assistant to
25  prescribe Schedule II controlled substances, if all of the
26  following conditions apply:

 

 

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1  (A) Specific Schedule II controlled substances by
2  oral dosage or topical or transdermal application may
3  be delegated, provided that the delegated Schedule II
4  controlled substances are routinely prescribed by the
5  collaborating physician. This delegation must identify
6  the specific Schedule II controlled substances by
7  either brand name or generic name. Schedule II
8  controlled substances to be delivered by injection or
9  other route of administration may not be delegated.
10  (B) (Blank).
11  (C) Any prescription must be limited to no more
12  than a 30-day supply, with any continuation authorized
13  only after prior approval of the collaborating
14  physician.
15  (D) The physician assistant must discuss the
16  condition of any patients for whom a controlled
17  substance is prescribed monthly with the collaborating
18  physician.
19  (E) The physician assistant meets the education
20  requirements of Section 303.05 of the Illinois
21  Controlled Substances Act.
22  (c) Nothing in this Act shall be construed to limit the
23  delegation of tasks or duties by a physician to a licensed
24  practical nurse, a registered professional nurse, or other
25  persons. Nothing in this Act shall be construed to limit the
26  method of delegation that may be authorized by any means,

 

 

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1  including, but not limited to, oral, written, electronic,
2  standing orders, protocols, guidelines, or verbal orders.
3  Nothing in this Act shall be construed to authorize a
4  physician assistant to provide health care services required
5  by law or rule to be performed by a physician. Nothing in this
6  Act shall be construed to authorize the delegation or
7  performance of operative surgery. Nothing in this Section
8  shall be construed to preclude a physician assistant from
9  assisting in surgery.
10  (c-5) Nothing in this Section shall be construed to apply
11  to any medication authority, including Schedule II controlled
12  substances of a licensed physician assistant for care provided
13  in a hospital, hospital affiliate, or ambulatory surgical
14  treatment center pursuant to Section 7.7 of this Act.
15  (d) (Blank).
16  (e) Nothing in this Section shall be construed to prohibit
17  generic substitution.
18  (Source: P.A. 101-13, eff. 6-12-19; 102-558, eff. 8-20-21;
19  revised 9-21-23.)
20  (Text of Section after amendment by P.A. 103-65)
21  (Section scheduled to be repealed on January 1, 2028)
22  Sec. 7.5. Written collaborative agreements; prescriptive
23  authority.
24  (a) A written collaborative agreement is required for all
25  physician assistants to practice in the State, except as

 

 

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1  provided in Sections Section 7.7 and 7.9 of this Act. When a
2  written collaborative agreement is required under this Act,
3  the following shall apply:
4  (1) A written collaborative agreement shall describe
5  the working relationship of the physician assistant with
6  the collaborating physician and shall describe the
7  categories of care, treatment, or procedures to be
8  provided by the physician assistant. The written
9  collaborative agreement shall promote the exercise of
10  professional judgment by the physician assistant
11  commensurate with his or her education and experience. The
12  services to be provided by the physician assistant shall
13  be services that the collaborating physician is authorized
14  to and generally provides to his or her patients in the
15  normal course of his or her clinical medical practice. The
16  written collaborative agreement need not describe the
17  exact steps that a physician assistant must take with
18  respect to each specific condition, disease, or symptom
19  but must specify which authorized procedures require the
20  presence of the collaborating physician as the procedures
21  are being performed. The relationship under a written
22  collaborative agreement shall not be construed to require
23  the personal presence of a physician at the place where
24  services are rendered. Methods of communication shall be
25  available for consultation with the collaborating
26  physician in person or by telecommunications or electronic

 

 

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1  communications as set forth in the written collaborative
2  agreement. For the purposes of this Act, "generally
3  provides to his or her patients in the normal course of his
4  or her clinical medical practice" means services, not
5  specific tasks or duties, the collaborating physician
6  routinely provides individually or through delegation to
7  other persons so that the physician has the experience and
8  ability to collaborate and provide consultation.
9  (2) (Blank). The written collaborative agreement shall
10  be adequate if a physician does each of the following:
11  (A) Participates in the joint formulation and
12  joint approval of orders or guidelines with the
13  physician assistant and he or she periodically reviews
14  such orders and the services provided patients under
15  such orders in accordance with accepted standards of
16  medical practice and physician assistant practice.
17  (B) Provides consultation at least once a month.
18  (3) A copy of the signed, written collaborative
19  agreement must be available to the Department upon request
20  from both the physician assistant and the collaborating
21  physician.
22  (4) A physician assistant shall inform each
23  collaborating physician of all written collaborative
24  agreements he or she has signed and provide a copy of these
25  to any collaborating physician upon request.
26  (b) To prescribe Schedule II, III, IV, or V controlled

 

 

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1  substances under this Section, a physician assistant must
2  obtain a mid-level practitioner controlled substances license.
3  A collaborating physician may, but is not required to,
4  delegate prescriptive authority to a physician assistant as
5  part of a written collaborative agreement. This authority may,
6  but is not required to, include prescription of, selection of,
7  orders for, administration of, storage of, acceptance of
8  samples of, and dispensing medical devices, over the counter
9  medications, legend drugs, medical gases, and controlled
10  substances categorized as Schedule II through V controlled
11  substances, as defined in Article II of the Illinois
12  Controlled Substances Act, and other preparations, including,
13  but not limited to, botanical and herbal remedies. The
14  collaborating physician must have a valid, current Illinois
15  controlled substance license and federal registration with the
16  Drug Enforcement Administration to delegate the authority to
17  prescribe controlled substances.
18  (1) To prescribe Schedule II, III, IV, or V controlled
19  substances under this Section, a physician assistant must
20  obtain a mid-level practitioner controlled substances
21  license. Medication orders issued by a physician assistant
22  shall be reviewed periodically by the collaborating
23  physician.
24  (2) The collaborating physician shall file with the
25  Department notice of delegation of prescriptive authority
26  to a physician assistant and termination of delegation,

 

 

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1  specifying the authority delegated or terminated. Upon
2  receipt of this notice delegating authority to prescribe
3  controlled substances, the physician assistant shall be
4  eligible to register for a mid-level practitioner
5  controlled substances license under Section 303.05 of the
6  Illinois Controlled Substances Act. Nothing in this Act
7  shall be construed to limit the delegation of tasks or
8  duties by the collaborating physician to a nurse or other
9  appropriately trained persons in accordance with Section
10  54.2 of the Medical Practice Act of 1987.
11  (3) In addition to the requirements of this subsection
12  (b), a collaborating physician may, but is not required
13  to, delegate authority to a physician assistant to
14  prescribe Schedule II controlled substances, if all of the
15  following conditions apply:
16  (A) Specific Schedule II controlled substances by
17  oral dosage or topical or transdermal application may
18  be delegated, provided that the delegated Schedule II
19  controlled substances are routinely prescribed by the
20  collaborating physician. This delegation must identify
21  the specific Schedule II controlled substances by
22  either brand name or generic name. Schedule II
23  controlled substances to be delivered by injection or
24  other route of administration may not be delegated.
25  (B) (Blank).
26  (C) Any prescription must be limited to no more

 

 

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1  than a 30-day supply, with any continuation authorized
2  only after prior approval of the collaborating
3  physician.
4  (D) The physician assistant must discuss the
5  condition of any patients for whom a controlled
6  substance is prescribed monthly with the collaborating
7  physician.
8  (E) The physician assistant meets the education
9  requirements of Section 303.05 of the Illinois
10  Controlled Substances Act.
11  (c) Nothing in this Act shall be construed to limit the
12  delegation of tasks or duties by a physician to a licensed
13  practical nurse, a registered professional nurse, or other
14  persons. Nothing in this Act shall be construed to limit the
15  method of delegation that may be authorized by any means,
16  including, but not limited to, oral, written, electronic,
17  standing orders, protocols, guidelines, or verbal orders.
18  Nothing in this Act shall be construed to authorize a
19  physician assistant to provide health care services required
20  by law or rule to be performed by a physician. Nothing in this
21  Act shall be construed to authorize the delegation or
22  performance of operative surgery. Nothing in this Section
23  shall be construed to preclude a physician assistant from
24  assisting in surgery.
25  (c-5) Nothing in this Section shall be construed to apply
26  to any medication authority, including Schedule II controlled

 

 

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1  substances of a licensed physician assistant for care provided
2  in a hospital, hospital affiliate, federally qualified health
3  center, or ambulatory surgical treatment center pursuant to
4  Section 7.7 of this Act, or to a physician assistant
5  satisfying the requirements of Section 7.9.
6  (d) (Blank).
7  (e) Nothing in this Section shall be construed to prohibit
8  generic substitution.
9  (f) Delegation of prescriptive authority by a physician is
10  not required under this Section.
11  (Source: P.A. 102-558, eff. 8-20-21; 103-65, eff. 1-1-24;
12  revised 9-21-23.)
13  (225 ILCS 95/7.7)
14  (Text of Section before amendment by P.A. 103-65)
15  (Section scheduled to be repealed on January 1, 2028)
16  Sec. 7.7. Physician assistants in hospitals, hospital
17  affiliates, or ambulatory surgical treatment centers.
18  (a) A physician assistant may provide services in a
19  hospital as defined in the Hospital Licensing Act, a hospital
20  affiliate as defined in the University of Illinois Hospital
21  Act, or a licensed ambulatory surgical treatment center as
22  defined in the Ambulatory Surgical Treatment Center Act
23  without a written collaborative agreement pursuant to Section
24  7.5 of this Act. A physician assistant must possess clinical
25  privileges recommended by the hospital medical staff and

 

 

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1  granted by the hospital or the consulting medical staff
2  committee and ambulatory surgical treatment center in order to
3  provide services. The medical staff or consulting medical
4  staff committee shall periodically review the services of
5  physician assistants granted clinical privileges, including
6  any care provided in a hospital affiliate. Authority may also
7  be granted when recommended by the hospital medical staff and
8  granted by the hospital or recommended by the consulting
9  medical staff committee and ambulatory surgical treatment
10  center to individual physician assistants to select, order,
11  and administer medications, including controlled substances,
12  to provide delineated care. In a hospital, hospital affiliate,
13  or ambulatory surgical treatment center, the attending
14  physician shall determine a physician assistant's role in
15  providing care for his or her patients, except as otherwise
16  provided in the medical staff bylaws or consulting committee
17  policies.
18  (a-5) Physician assistants practicing in a hospital
19  affiliate may be, but are not required to be, granted
20  authority to prescribe Schedule II through V controlled
21  substances when such authority is recommended by the
22  appropriate physician committee of the hospital affiliate and
23  granted by the hospital affiliate. This authority may, but is
24  not required to, include prescription of, selection of, orders
25  for, administration of, storage of, acceptance of samples of,
26  and dispensing over-the-counter medications, legend drugs,

 

 

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1  medical gases, and controlled substances categorized as
2  Schedule II through V controlled substances, as defined in
3  Article II of the Illinois Controlled Substances Act, and
4  other preparations, including, but not limited to, botanical
5  and herbal remedies.
6  To prescribe controlled substances under this subsection
7  (a-5), a physician assistant must obtain a mid-level
8  practitioner controlled substance license. Medication orders
9  shall be reviewed periodically by the appropriate hospital
10  affiliate physicians committee or its physician designee.
11  The hospital affiliate shall file with the Department
12  notice of a grant of prescriptive authority consistent with
13  this subsection (a-5) and termination of such a grant of
14  authority in accordance with rules of the Department. Upon
15  receipt of this notice of grant of authority to prescribe any
16  Schedule II through V controlled substances, the licensed
17  physician assistant may register for a mid-level practitioner
18  controlled substance license under Section 303.05 of the
19  Illinois Controlled Substances Act.
20  In addition, a hospital affiliate may, but is not required
21  to, grant authority to a physician assistant to prescribe any
22  Schedule II controlled substances if all of the following
23  conditions apply:
24  (1) specific Schedule II controlled substances by oral
25  dosage or topical or transdermal application may be
26  designated, provided that the designated Schedule II

 

 

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1  controlled substances are routinely prescribed by
2  physician assistants in their area of certification; this
3  grant of authority must identify the specific Schedule II
4  controlled substances by either brand name or generic
5  name; authority to prescribe or dispense Schedule II
6  controlled substances to be delivered by injection or
7  other route of administration may not be granted;
8  (2) any grant of authority must be controlled
9  substances limited to the practice of the physician
10  assistant;
11  (3) any prescription must be limited to no more than a
12  30-day supply;
13  (4) the physician assistant must discuss the condition
14  of any patients for whom a controlled substance is
15  prescribed monthly with the appropriate physician
16  committee of the hospital affiliate or its physician
17  designee; and
18  (5) the physician assistant must meet the education
19  requirements of Section 303.05 of the Illinois Controlled
20  Substances Act.
21  (b) A physician assistant granted authority to order
22  medications including controlled substances may complete
23  discharge prescriptions provided the prescription is in the
24  name of the physician assistant and the attending or
25  discharging physician.
26  (c) Physician assistants practicing in a hospital,

 

 

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1  hospital affiliate, or an ambulatory surgical treatment center
2  are not required to obtain a mid-level controlled substance
3  license to order controlled substances under Section 303.05 of
4  the Illinois Controlled Substances Act.
5  (Source: P.A. 100-453, eff. 8-25-17.)
6  (Text of Section after amendment by P.A. 103-65)
7  (Section scheduled to be repealed on January 1, 2028)
8  Sec. 7.7. Physician assistants in hospitals, hospital
9  affiliates, federally qualified health centers, or ambulatory
10  surgical treatment centers.
11  (a) A physician assistant may provide services in a
12  hospital as defined in the Hospital Licensing Act, a hospital
13  affiliate as defined in the University of Illinois Hospital
14  Act, a federally qualified health center, or a licensed
15  ambulatory surgical treatment center as defined in the
16  Ambulatory Surgical Treatment Center Act without a written
17  collaborative agreement pursuant to Section 7.5 of this Act
18  only in accordance with this Section. A physician assistant
19  must possess clinical privileges recommended by (i) the
20  hospital medical staff and granted by the hospital, (ii) the
21  physician committee and federally qualified health center, or
22  (iii) the consulting medical staff committee and ambulatory
23  surgical treatment center in order to provide services. The
24  medical staff, physician committee, or consulting medical
25  staff committee shall periodically review the services of

 

 

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1  physician assistants granted clinical privileges, including
2  any care provided in a hospital affiliate or federally
3  qualified health center. A physician assistant practicing
4  under this Section may prescribe, select, order, and
5  administer medications, including controlled substances.
6  Authority may also be granted when recommended by the hospital
7  medical staff and granted by the hospital, recommended by the
8  physician committee and granted by the federally qualified
9  health center, or recommended by the consulting medical staff
10  committee and ambulatory surgical treatment center to
11  individual physician assistants to select, order, and
12  administer medications, including controlled substances, to
13  provide delineated care. In a hospital, hospital affiliate,
14  federally qualified health center, or ambulatory surgical
15  treatment center, the attending physician shall determine a
16  physician assistant's role in providing care for his or her
17  patients, except as otherwise provided in the medical staff
18  bylaws or consulting committee policies.
19  (a-5) Physician assistants practicing in a hospital
20  affiliate or a federally qualified health center may be, but
21  are not required to be, granted authority to prescribe
22  Schedule II through V controlled substances when such
23  authority is recommended by the appropriate physician
24  committee of the hospital affiliate and granted by the
25  hospital affiliate or recommended by the physician committee
26  of the federally qualified health center and granted by the

 

 

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1  federally qualified health center. This authority may, but is
2  not required to, include prescription of, selection of, orders
3  for, administration of, storage of, acceptance of samples of,
4  and dispensing over-the-counter medications, legend drugs,
5  medical gases, and controlled substances categorized as
6  Schedule II through V controlled substances, as defined in
7  Article II of the Illinois Controlled Substances Act, and
8  other preparations, including, but not limited to, botanical
9  and herbal remedies.
10  To prescribe controlled substances under this subsection
11  (a-5), a physician assistant must obtain a mid-level
12  practitioner controlled substance license. Medication orders
13  shall be reviewed periodically by the appropriate hospital
14  affiliate physicians committee or its physician designee or by
15  the physician committee of a federally qualified health
16  center.
17  The hospital affiliate or federally qualified health
18  center shall file with the Department notice of a grant of
19  prescriptive authority consistent with this subsection (a-5)
20  and termination of such a grant of authority in accordance
21  with rules of the Department. Upon receipt of this notice of
22  grant of authority to prescribe any Schedule II through V
23  controlled substances, the licensed physician assistant may
24  register for a mid-level practitioner controlled substance
25  license under Section 303.05 of the Illinois Controlled
26  Substances Act.

 

 

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1  In addition, a hospital affiliate or a federally qualified
2  health center may, but is not required to, grant authority to a
3  physician assistant to prescribe any Schedule II controlled
4  substances if all of the following conditions apply:
5  (1) specific Schedule II controlled substances by oral
6  dosage or topical or transdermal application may be
7  designated, provided that the designated Schedule II
8  controlled substances are routinely prescribed by
9  physician assistants in their area of certification; this
10  grant of authority must identify the specific Schedule II
11  controlled substances by either brand name or generic
12  name; authority to prescribe or dispense Schedule II
13  controlled substances to be delivered by injection or
14  other route of administration may not be granted;
15  (2) any grant of authority must be controlled
16  substances limited to the practice of the physician
17  assistant;
18  (3) any prescription must be limited to no more than a
19  30-day supply;
20  (4) the physician assistant must discuss the condition
21  of any patients for whom a controlled substance is
22  prescribed monthly with the appropriate physician
23  committee of the hospital affiliate or its physician
24  designee, or the physician committee of a federally
25  qualified health center; and
26  (5) the physician assistant must meet the education

 

 

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1  requirements of Section 303.05 of the Illinois Controlled
2  Substances Act.
3  (b) A physician assistant granted authority to order
4  medications including controlled substances may complete
5  discharge prescriptions provided the prescription is in the
6  name of the physician assistant and the attending or
7  discharging physician.
8  (c) Physician assistants practicing in a hospital,
9  hospital affiliate, federally qualified health center, or an
10  ambulatory surgical treatment center are not required to
11  obtain a mid-level controlled substance license to order
12  controlled substances under Section 303.05 of the Illinois
13  Controlled Substances Act.
14  (d) Delegation of prescriptive authority by a physician is
15  not required under this Section.
16  (Source: P.A. 103-65, eff. 1-1-24.)
17  (225 ILCS 95/7.8 new)
18  Sec. 7.8. Prescriptive authority. A physician assistant
19  may prescribe, dispense, order, administer, and procure drugs
20  and medical devices without delegation of authority by a
21  physician. The prescriptive authority may include prescribing
22  Schedule II, III, IV, and V controlled substances. To
23  prescribe Schedule II, III, IV, or V controlled substances
24  under this Act, a physician assistant must obtain a mid-level
25  practitioner controlled substances license. When a written

 

 

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1  collaborative agreement is required under this Act, delegation
2  of prescriptive authority by a physician is not required.
3  (225 ILCS 95/7.9 new)
4  Sec. 7.9. Optimal practice.
5  (a) A physician assistant may practice without a written
6  collaborative agreement as described in this Section.
7  (b) A physician assistant who files with the Department a
8  notarized attestation of completion of at least 250 hours of
9  continuing education or training and at least 2,000 hours of
10  clinical experience after first attaining national
11  certification shall not require a written collaborative
12  agreement. Documentation of successful completion shall be
13  provided to the Department upon request.
14  (c) The scope of practice of a physician assistant with
15  optimal practice includes:
16  (1) all matters defined as physician assistant
17  practice;
18  (2) practicing without a written collaborative
19  agreement in all practice settings consistent with this
20  Act;
21  (3) authority to prescribe both legend drugs and
22  Schedule II through V controlled substances, including
23  prescription of, selection of, orders for, administration
24  of, storage of, acceptance of samples of, and dispensing
25  over-the-counter medications, legend drugs, and controlled

 

 

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1  substances categorized as any Schedule II through V
2  controlled substances, as defined in Article II of the
3  Illinois Controlled Substances Act, and other
4  preparations, including, but not limited to, botanical and
5  herbal remedies; and
6  (4) authority to obtain an Illinois controlled
7  substance license and a federal Drug Enforcement
8  Administration number.
9  The scope of practice of a physician assistant does not
10  include operative surgery. Nothing in this Section shall be
11  construed to preclude a physician assistant from assisting in
12  surgery or performing other procedures as privileged by the
13  physician assistant's employer.
14  (d) The Department may adopt rules necessary to administer
15  this Section, including, but not limited to, requiring the
16  completion of forms and the payment of fees.
17  (e) Nothing in this Section shall be construed to prohibit
18  a physician assistant's employer from requiring a physician
19  assistant who satisfies the qualifications of subsection (b)
20  to practice with a written collaborative agreement.
21  (f) Nothing in this Act shall be construed to authorize a
22  physician assistant with optimal practice authority to provide
23  health care services required by law or rule to be performed by
24  a physician.
25  (225 ILCS 95/17) (from Ch. 111, par. 4617)

 

 

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1  (Section scheduled to be repealed on January 1, 2028)
2  Sec. 17. Inactive status. Any physician assistant who
3  notified the Department in writing on forms prescribed by the
4  Department, may elect to place his or her license on an
5  inactive status and shall, subject to rules of the Department,
6  be excused from payment of renewal fees until he or she
7  notifies the Department in writing of his or her intention to
8  restore the license. Any person who holds an active license or
9  permit issued under the Medical Practice Act of 1987 shall
10  have that license or permit automatically placed into inactive
11  status upon issuance of a physician assistant license. Any
12  person who holds an active license as a physician assistant
13  who is issued a license or permit under the Medical Practice
14  Act of 1987 shall have the physician assistant license
15  automatically placed into inactive status.
16  Any physician assistant requesting restoration from
17  inactive status shall be required to pay the current renewal
18  fee and shall be required to restore his or her license, as
19  provided in Section 16 of this Act.
20  Any physician assistant whose license is in an inactive
21  status shall not practice in the State of Illinois.
22  Any licensee who shall engage in practice while his or her
23  license is lapsed or on inactive status shall be considered to
24  be practicing without a license, which shall be grounds for
25  discipline under Section 21 of this Act.
26  (Source: P.A. 90-61, eff. 12-30-97.)

 

 

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1  (225 ILCS 95/20) (from Ch. 111, par. 4620)
2  (Section scheduled to be repealed on January 1, 2028)
3  Sec. 20. Limitations.
4  (a) No corporation, which stated purpose includes, or
5  which practices, or which holds itself out as available to
6  practice as a physician assistant or to practice any of the
7  functions described in Section 4 of this Act, shall be issued a
8  license by the Department, nor shall the Secretary of State
9  approve or accept articles of incorporation for such a
10  corporation.
11  (b) Pursuant to subparagraph (a) of paragraph (2) of
12  Section 3.6 of the Professional Service Corporation Act and
13  Section 2 of the Medical Corporation Act, a person licensed
14  under this Act may not own a corporation for the purposes of
15  practicing medicine.
16  (c) Pursuant to paragraph (2) of subsection (a) of Section
17  13 of the Professional Limited Liability Company Act, a person
18  licensed under this Act may not own a professional limited
19  liability company for the purposes of practicing medicine.
20  (Source: P.A. 85-981.)
21  (225 ILCS 95/21) (from Ch. 111, par. 4621)
22  (Section scheduled to be repealed on January 1, 2028)
23  Sec. 21. Grounds for disciplinary action.
24  (a) The Department may refuse to issue or to renew, or may

 

 

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1  revoke, suspend, place on probation, reprimand, or take other
2  disciplinary or non-disciplinary action with regard to any
3  license issued under this Act as the Department may deem
4  proper, including the issuance of fines not to exceed $10,000
5  for each violation, for any one or combination of the
6  following causes:
7  (1) Material misstatement in furnishing information to
8  the Department.
9  (2) Violations of this Act, or the rules adopted under
10  this Act.
11  (3) Conviction by plea of guilty or nolo contendere,
12  finding of guilt, jury verdict, or entry of judgment or
13  sentencing, including, but not limited to, convictions,
14  preceding sentences of supervision, conditional discharge,
15  or first offender probation, under the laws of any
16  jurisdiction of the United States that is: (i) a felony;
17  or (ii) a misdemeanor, an essential element of which is
18  dishonesty, or that is directly related to the practice of
19  the profession.
20  (4) Making any misrepresentation for the purpose of
21  obtaining licenses.
22  (5) Professional incompetence.
23  (6) Aiding or assisting another person in violating
24  any provision of this Act or its rules.
25  (7) Failing, within 60 days, to provide information in
26  response to a written request made by the Department.

 

 

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1  (8) Engaging in dishonorable, unethical, or
2  unprofessional conduct, as defined by rule, of a character
3  likely to deceive, defraud, or harm the public.
4  (9) Habitual or excessive use or addiction to alcohol,
5  narcotics, stimulants, or any other chemical agent or drug
6  that results in a physician assistant's inability to
7  practice with reasonable judgment, skill, or safety.
8  (10) Discipline by another U.S. jurisdiction or
9  foreign nation, if at least one of the grounds for
10  discipline is the same or substantially equivalent to
11  those set forth in this Section.
12  (11) Directly or indirectly giving to or receiving
13  from any person, firm, corporation, partnership, or
14  association any fee, commission, rebate or other form of
15  compensation for any professional services not actually or
16  personally rendered. Nothing in this paragraph (11)
17  affects any bona fide independent contractor or employment
18  arrangements, which may include provisions for
19  compensation, health insurance, pension, or other
20  employment benefits, with persons or entities authorized
21  under this Act for the provision of services within the
22  scope of the licensee's practice under this Act.
23  (12) A finding by the Board that the licensee, after
24  having his or her license placed on probationary status,
25  has violated the terms of probation.
26  (13) Abandonment of a patient.

 

 

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1  (14) Willfully making or filing false records or
2  reports in his or her practice, including, but not limited
3  to, false records filed with State agencies or
4  departments.
5  (15) Willfully failing to report an instance of
6  suspected child abuse or neglect as required by the Abused
7  and Neglected Child Reporting Act.
8  (16) Physical illness, or mental illness or impairment
9  that results in the inability to practice the profession
10  with reasonable judgment, skill, or safety, including, but
11  not limited to, deterioration through the aging process or
12  loss of motor skill.
13  (17) Being named as a perpetrator in an indicated
14  report by the Department of Children and Family Services
15  under the Abused and Neglected Child Reporting Act, and
16  upon proof by clear and convincing evidence that the
17  licensee has caused a child to be an abused child or
18  neglected child as defined in the Abused and Neglected
19  Child Reporting Act.
20  (18) (Blank).
21  (19) Gross negligence resulting in permanent injury or
22  death of a patient.
23  (20) Employment of fraud, deception or any unlawful
24  means in applying for or securing a license as a physician
25  assistant.
26  (21) Exceeding the authority delegated to him or her

 

 

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1  by his or her collaborating physician in a written
2  collaborative agreement, when the agreement is required
3  under this Act.
4  (22) Immoral conduct in the commission of any act,
5  such as sexual abuse, sexual misconduct, or sexual
6  exploitation related to the licensee's practice.
7  (23) Violation of the Health Care Worker Self-Referral
8  Act.
9  (24) Practicing under a false or assumed name, except
10  as provided by law.
11  (25) Making a false or misleading statement regarding
12  his or her skill or the efficacy or value of the medicine,
13  treatment, or remedy prescribed by him or her in the
14  course of treatment.
15  (26) Allowing another person to use his or her license
16  to practice.
17  (27) Prescribing, selling, administering,
18  distributing, giving, or self-administering a drug
19  classified as a controlled substance for other than
20  medically accepted therapeutic purposes.
21  (28) Promotion of the sale of drugs, devices,
22  appliances, or goods provided for a patient in a manner to
23  exploit the patient for financial gain.
24  (29) A pattern of practice or other behavior that
25  demonstrates incapacity or incompetence to practice under
26  this Act.

 

 

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1  (30) Violating State or federal laws or regulations
2  relating to controlled substances or other legend drugs or
3  ephedra as defined in the Ephedra Prohibition Act.
4  (31) (Blank). Exceeding the prescriptive authority
5  delegated by the collaborating physician or violating the
6  written collaborative agreement delegating that authority.
7  (32) (Blank). Practicing without providing to the
8  Department a notice of collaboration or delegation of
9  prescriptive authority.
10  (33) Failure to establish and maintain records of
11  patient care and treatment as required by law.
12  (34) Attempting to subvert or cheat on the examination
13  of the National Commission on Certification of Physician
14  Assistants or its successor agency.
15  (35) Willfully or negligently violating the
16  confidentiality between physician assistant and patient,
17  except as required by law.
18  (36) Willfully failing to report an instance of
19  suspected abuse, neglect, financial exploitation, or
20  self-neglect of an eligible adult as defined in and
21  required by the Adult Protective Services Act.
22  (37) Being named as an abuser in a verified report by
23  the Department on Aging under the Adult Protective
24  Services Act and upon proof by clear and convincing
25  evidence that the licensee abused, neglected, or
26  financially exploited an eligible adult as defined in the

 

 

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1  Adult Protective Services Act.
2  (38) Failure to report to the Department an adverse
3  final action taken against him or her by another licensing
4  jurisdiction of the United States or a foreign state or
5  country, a peer review body, a health care institution, a
6  professional society or association, a governmental
7  agency, a law enforcement agency, or a court acts or
8  conduct similar to acts or conduct that would constitute
9  grounds for action under this Section.
10  (39) Failure to provide copies of records of patient
11  care or treatment, except as required by law.
12  (40) (Blank). Entering into an excessive number of
13  written collaborative agreements with licensed physicians
14  resulting in an inability to adequately collaborate.
15  (41) (Blank). Repeated failure to adequately
16  collaborate with a collaborating physician.
17  (42) Violating the Compassionate Use of Medical
18  Cannabis Program Act.
19  (b) The Department may, without a hearing, refuse to issue
20  or renew or may suspend the license of any person who fails to
21  file a return, or to pay the tax, penalty or interest shown in
22  a filed return, or to pay any final assessment of the tax,
23  penalty, or interest as required by any tax Act administered
24  by the Illinois Department of Revenue, until such time as the
25  requirements of any such tax Act are satisfied.
26  (b-5) The Department shall not revoke, suspend, summarily

 

 

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1  suspend, place on prohibition, reprimand, refuse to issue or
2  renew, or take any other disciplinary or non-disciplinary
3  action against the license or permit issued under this Act to
4  practice as a physician assistant based solely upon the
5  physician assistant providing, authorizing, recommending,
6  aiding, assisting, referring for, or otherwise participating
7  in any health care service, so long as the care was not
8  unlawful under the laws of this State, regardless of whether
9  the patient was a resident of this State or another state.
10  (b-10) The Department shall not revoke, suspend, summarily
11  suspend, place on prohibition, reprimand, refuse to issue or
12  renew, or take any other disciplinary or non-disciplinary
13  action against the license or permit issued under this Act to
14  practice as a physician assistant based upon the physician
15  assistant's license being revoked or suspended, or the
16  physician assistant being otherwise disciplined by any other
17  state, if that revocation, suspension, or other form of
18  discipline was based solely on the physician assistant
19  violating another state's laws prohibiting the provision of,
20  authorization of, recommendation of, aiding or assisting in,
21  referring for, or participation in any health care service if
22  that health care service as provided would not have been
23  unlawful under the laws of this State and is consistent with
24  the standards of conduct for a physician assistant practicing
25  in Illinois.
26  (b-15) The conduct specified in subsections (b-5) and

 

 

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1  (b-10) shall not constitute grounds for suspension under
2  Section 22.13.
3  (b-20) An applicant seeking licensure, certification, or
4  authorization pursuant to this Act who has been subject to
5  disciplinary action by a duly authorized professional
6  disciplinary agency of another jurisdiction solely on the
7  basis of having provided, authorized, recommended, aided,
8  assisted, referred for, or otherwise participated in health
9  care shall not be denied such licensure, certification, or
10  authorization, unless the Department determines that such
11  action would have constituted professional misconduct in this
12  State; however, nothing in this Section shall be construed as
13  prohibiting the Department from evaluating the conduct of such
14  applicant and making a determination regarding the licensure,
15  certification, or authorization to practice a profession under
16  this Act.
17  (c) The determination by a circuit court that a licensee
18  is subject to involuntary admission or judicial admission as
19  provided in the Mental Health and Developmental Disabilities
20  Code operates as an automatic suspension. The suspension will
21  end only upon a finding by a court that the patient is no
22  longer subject to involuntary admission or judicial admission
23  and issues an order so finding and discharging the patient,
24  and upon the recommendation of the Board to the Secretary that
25  the licensee be allowed to resume his or her practice.
26  (d) In enforcing this Section, the Department upon a

 

 

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1  showing of a possible violation may compel an individual
2  licensed to practice under this Act, or who has applied for
3  licensure under this Act, to submit to a mental or physical
4  examination, or both, which may include a substance abuse or
5  sexual offender evaluation, as required by and at the expense
6  of the Department.
7  The Department shall specifically designate the examining
8  physician licensed to practice medicine in all of its branches
9  or, if applicable, the multidisciplinary team involved in
10  providing the mental or physical examination or both. The
11  multidisciplinary team shall be led by a physician licensed to
12  practice medicine in all of its branches and may consist of one
13  or more or a combination of physicians licensed to practice
14  medicine in all of its branches, licensed clinical
15  psychologists, licensed clinical social workers, licensed
16  clinical professional counselors, and other professional and
17  administrative staff. Any examining physician or member of the
18  multidisciplinary team may require any person ordered to
19  submit to an examination pursuant to this Section to submit to
20  any additional supplemental testing deemed necessary to
21  complete any examination or evaluation process, including, but
22  not limited to, blood testing, urinalysis, psychological
23  testing, or neuropsychological testing.
24  The Department may order the examining physician or any
25  member of the multidisciplinary team to provide to the
26  Department any and all records, including business records,

 

 

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1  that relate to the examination and evaluation, including any
2  supplemental testing performed.
3  The Department may order the examining physician or any
4  member of the multidisciplinary team to present testimony
5  concerning the mental or physical examination of the licensee
6  or applicant. No information, report, record, or other
7  documents in any way related to the examination shall be
8  excluded by reason of any common law or statutory privilege
9  relating to communications between the licensee or applicant
10  and the examining physician or any member of the
11  multidisciplinary team. No authorization is necessary from the
12  licensee or applicant ordered to undergo an examination for
13  the examining physician or any member of the multidisciplinary
14  team to provide information, reports, records, or other
15  documents or to provide any testimony regarding the
16  examination and evaluation.
17  The individual to be examined may have, at his or her own
18  expense, another physician of his or her choice present during
19  all aspects of this examination. However, that physician shall
20  be present only to observe and may not interfere in any way
21  with the examination.
22  Failure of an individual to submit to a mental or physical
23  examination, when ordered, shall result in an automatic
24  suspension of his or her license until the individual submits
25  to the examination.
26  If the Department finds an individual unable to practice

 

 

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1  because of the reasons set forth in this Section, the
2  Department may require that individual to submit to care,
3  counseling, or treatment by physicians approved or designated
4  by the Department, as a condition, term, or restriction for
5  continued, reinstated, or renewed licensure to practice; or,
6  in lieu of care, counseling, or treatment, the Department may
7  file a complaint to immediately suspend, revoke, or otherwise
8  discipline the license of the individual. An individual whose
9  license was granted, continued, reinstated, renewed,
10  disciplined, or supervised subject to such terms, conditions,
11  or restrictions, and who fails to comply with such terms,
12  conditions, or restrictions, shall be referred to the
13  Secretary for a determination as to whether the individual
14  shall have his or her license suspended immediately, pending a
15  hearing by the Department.
16  In instances in which the Secretary immediately suspends a
17  person's license under this Section, a hearing on that
18  person's license must be convened by the Department within 30
19  days after the suspension and completed without appreciable
20  delay. The Department shall have the authority to review the
21  subject individual's record of treatment and counseling
22  regarding the impairment to the extent permitted by applicable
23  federal statutes and regulations safeguarding the
24  confidentiality of medical records.
25  An individual licensed under this Act and affected under
26  this Section shall be afforded an opportunity to demonstrate

 

 

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1  to the Department that he or she can resume practice in
2  compliance with acceptable and prevailing standards under the
3  provisions of his or her license.
4  (e) An individual or organization acting in good faith,
5  and not in a willful and wanton manner, in complying with this
6  Section by providing a report or other information to the
7  Board, by assisting in the investigation or preparation of a
8  report or information, by participating in proceedings of the
9  Board, or by serving as a member of the Board, shall not be
10  subject to criminal prosecution or civil damages as a result
11  of such actions.
12  (f) Members of the Board shall be indemnified by the State
13  for any actions occurring within the scope of services on the
14  Board, done in good faith and not willful and wanton in nature.
15  The Attorney General shall defend all such actions unless he
16  or she determines either that there would be a conflict of
17  interest in such representation or that the actions complained
18  of were not in good faith or were willful and wanton.
19  If the Attorney General declines representation, the
20  member has the right to employ counsel of his or her choice,
21  whose fees shall be provided by the State, after approval by
22  the Attorney General, unless there is a determination by a
23  court that the member's actions were not in good faith or were
24  willful and wanton.
25  The member must notify the Attorney General within 7 days
26  after receipt of notice of the initiation of any action

 

 

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1  involving services of the Board. Failure to so notify the
2  Attorney General constitutes an absolute waiver of the right
3  to a defense and indemnification.
4  The Attorney General shall determine, within 7 days after
5  receiving such notice, whether he or she will undertake to
6  represent the member.
7  (g) The Department may adopt rules to implement the
8  changes made by this amendatory Act of the 102nd General
9  Assembly.
10  (Source: P.A. 101-363, eff. 8-9-19; 102-558, eff. 8-20-21;
11  102-1117, eff. 1-13-23.)
12  Section 10. The Illinois Controlled Substances Act is
13  amended by changing Sections 102 and 303.05 as follows:
14  (720 ILCS 570/102) (from Ch. 56 1/2, par. 1102)
15  Sec. 102. Definitions.  As used in this Act, unless the
16  context otherwise requires:
17  (a) "Addict" means any person who habitually uses any
18  drug, chemical, substance or dangerous drug other than alcohol
19  so as to endanger the public morals, health, safety or welfare
20  or who is so far addicted to the use of a dangerous drug or
21  controlled substance other than alcohol as to have lost the
22  power of self control with reference to his or her addiction.
23  (b) "Administer" means the direct application of a
24  controlled substance, whether by injection, inhalation,

 

 

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1  ingestion, or any other means, to the body of a patient,
2  research subject, or animal (as defined by the Humane
3  Euthanasia in Animal Shelters Act) by:
4  (1) a practitioner (or, in his or her presence, by his
5  or her authorized agent),
6  (2) the patient or research subject pursuant to an
7  order, or
8  (3) a euthanasia technician as defined by the Humane
9  Euthanasia in Animal Shelters Act.
10  (c) "Agent" means an authorized person who acts on behalf
11  of or at the direction of a manufacturer, distributor,
12  dispenser, prescriber, or practitioner. It does not include a
13  common or contract carrier, public warehouseman or employee of
14  the carrier or warehouseman.
15  (c-1) "Anabolic Steroids" means any drug or hormonal
16  substance, chemically and pharmacologically related to
17  testosterone (other than estrogens, progestins,
18  corticosteroids, and dehydroepiandrosterone), and includes:
19  (i) 3[beta],17-dihydroxy-5a-androstane,
20  (ii) 3[alpha],17[beta]-dihydroxy-5a-androstane,
21  (iii) 5[alpha]-androstan-3,17-dione,
22  (iv) 1-androstenediol (3[beta],
23  17[beta]-dihydroxy-5[alpha]-androst-1-ene),
24  (v) 1-androstenediol (3[alpha],
25  17[beta]-dihydroxy-5[alpha]-androst-1-ene),
26  (vi) 4-androstenediol

 

 

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1  (3[beta],17[beta]-dihydroxy-androst-4-ene),
2  (vii) 5-androstenediol
3  (3[beta],17[beta]-dihydroxy-androst-5-ene),
4  (viii) 1-androstenedione
5  ([5alpha]-androst-1-en-3,17-dione),
6  (ix) 4-androstenedione
7  (androst-4-en-3,17-dione),
8  (x) 5-androstenedione
9  (androst-5-en-3,17-dione),
10  (xi) bolasterone (7[alpha],17a-dimethyl-17[beta]-
11  hydroxyandrost-4-en-3-one),
12  (xii) boldenone (17[beta]-hydroxyandrost-
13  1,4,-diene-3-one),
14  (xiii) boldione (androsta-1,4-
15  diene-3,17-dione),
16  (xiv) calusterone (7[beta],17[alpha]-dimethyl-17
17  [beta]-hydroxyandrost-4-en-3-one),
18  (xv) clostebol (4-chloro-17[beta]-
19  hydroxyandrost-4-en-3-one),
20  (xvi) dehydrochloromethyltestosterone (4-chloro-
21  17[beta]-hydroxy-17[alpha]-methyl-
22  androst-1,4-dien-3-one),
23  (xvii) desoxymethyltestosterone
24  (17[alpha]-methyl-5[alpha]
25  -androst-2-en-17[beta]-ol)(a.k.a., madol),
26  (xviii) [delta]1-dihydrotestosterone (a.k.a.

 

 

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1  '1-testosterone') (17[beta]-hydroxy-
2  5[alpha]-androst-1-en-3-one),
3  (xix) 4-dihydrotestosterone (17[beta]-hydroxy-
4  androstan-3-one),
5  (xx) drostanolone (17[beta]-hydroxy-2[alpha]-methyl-
6  5[alpha]-androstan-3-one),
7  (xxi) ethylestrenol (17[alpha]-ethyl-17[beta]-
8  hydroxyestr-4-ene),
9  (xxii) fluoxymesterone (9-fluoro-17[alpha]-methyl-
10  1[beta],17[beta]-dihydroxyandrost-4-en-3-one),
11  (xxiii) formebolone (2-formyl-17[alpha]-methyl-11[alpha],
12  17[beta]-dihydroxyandrost-1,4-dien-3-one),
13  (xxiv) furazabol (17[alpha]-methyl-17[beta]-
14  hydroxyandrostano[2,3-c]-furazan),
15  (xxv) 13[beta]-ethyl-17[beta]-hydroxygon-4-en-3-one,
16  (xxvi) 4-hydroxytestosterone (4,17[beta]-dihydroxy-
17  androst-4-en-3-one),
18  (xxvii) 4-hydroxy-19-nortestosterone (4,17[beta]-
19  dihydroxy-estr-4-en-3-one),
20  (xxviii) mestanolone (17[alpha]-methyl-17[beta]-
21  hydroxy-5-androstan-3-one),
22  (xxix) mesterolone (1amethyl-17[beta]-hydroxy-
23  [5a]-androstan-3-one),
24  (xxx) methandienone (17[alpha]-methyl-17[beta]-
25  hydroxyandrost-1,4-dien-3-one),
26  (xxxi) methandriol (17[alpha]-methyl-3[beta],17[beta]-

 

 

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1  dihydroxyandrost-5-ene),
2  (xxxii) methenolone (1-methyl-17[beta]-hydroxy-
3  5[alpha]-androst-1-en-3-one),
4  (xxxiii) 17[alpha]-methyl-3[beta], 17[beta]-
5  dihydroxy-5a-androstane,
6  (xxxiv) 17[alpha]-methyl-3[alpha],17[beta]-dihydroxy
7  -5a-androstane,
8  (xxxv) 17[alpha]-methyl-3[beta],17[beta]-
9  dihydroxyandrost-4-ene),
10  (xxxvi) 17[alpha]-methyl-4-hydroxynandrolone (17[alpha]-
11  methyl-4-hydroxy-17[beta]-hydroxyestr-4-en-3-one),
12  (xxxvii) methyldienolone (17[alpha]-methyl-17[beta]-
13  hydroxyestra-4,9(10)-dien-3-one),
14  (xxxviii) methyltrienolone (17[alpha]-methyl-17[beta]-
15  hydroxyestra-4,9-11-trien-3-one),
16  (xxxix) methyltestosterone (17[alpha]-methyl-17[beta]-
17  hydroxyandrost-4-en-3-one),
18  (xl) mibolerone (7[alpha],17a-dimethyl-17[beta]-
19  hydroxyestr-4-en-3-one),
20  (xli) 17[alpha]-methyl-[delta]1-dihydrotestosterone
21  (17b[beta]-hydroxy-17[alpha]-methyl-5[alpha]-
22  androst-1-en-3-one)(a.k.a. '17-[alpha]-methyl-
23  1-testosterone'),
24  (xlii) nandrolone (17[beta]-hydroxyestr-4-en-3-one),
25  (xliii) 19-nor-4-androstenediol (3[beta], 17[beta]-
26  dihydroxyestr-4-ene),

 

 

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1  (xliv) 19-nor-4-androstenediol (3[alpha], 17[beta]-
2  dihydroxyestr-4-ene),
3  (xlv) 19-nor-5-androstenediol (3[beta], 17[beta]-
4  dihydroxyestr-5-ene),
5  (xlvi) 19-nor-5-androstenediol (3[alpha], 17[beta]-
6  dihydroxyestr-5-ene),
7  (xlvii) 19-nor-4,9(10)-androstadienedione
8  (estra-4,9(10)-diene-3,17-dione),
9  (xlviii) 19-nor-4-androstenedione (estr-4-
10  en-3,17-dione),
11  (xlix) 19-nor-5-androstenedione (estr-5-
12  en-3,17-dione),
13  (l) norbolethone (13[beta], 17a-diethyl-17[beta]-
14  hydroxygon-4-en-3-one),
15  (li) norclostebol (4-chloro-17[beta]-
16  hydroxyestr-4-en-3-one),
17  (lii) norethandrolone (17[alpha]-ethyl-17[beta]-
18  hydroxyestr-4-en-3-one),
19  (liii) normethandrolone (17[alpha]-methyl-17[beta]-
20  hydroxyestr-4-en-3-one),
21  (liv) oxandrolone (17[alpha]-methyl-17[beta]-hydroxy-
22  2-oxa-5[alpha]-androstan-3-one),
23  (lv) oxymesterone (17[alpha]-methyl-4,17[beta]-
24  dihydroxyandrost-4-en-3-one),
25  (lvi) oxymetholone (17[alpha]-methyl-2-hydroxymethylene-
26  17[beta]-hydroxy-(5[alpha]-androstan-3-one),

 

 

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1  (lvii) stanozolol (17[alpha]-methyl-17[beta]-hydroxy-
2  (5[alpha]-androst-2-eno[3,2-c]-pyrazole),
3  (lviii) stenbolone (17[beta]-hydroxy-2-methyl-
4  (5[alpha]-androst-1-en-3-one),
5  (lix) testolactone (13-hydroxy-3-oxo-13,17-
6  secoandrosta-1,4-dien-17-oic
7  acid lactone),
8  (lx) testosterone (17[beta]-hydroxyandrost-
9  4-en-3-one),
10  (lxi) tetrahydrogestrinone (13[beta], 17[alpha]-
11  diethyl-17[beta]-hydroxygon-
12  4,9,11-trien-3-one),
13  (lxii) trenbolone (17[beta]-hydroxyestr-4,9,
14  11-trien-3-one).
15  Any person who is otherwise lawfully in possession of an
16  anabolic steroid, or who otherwise lawfully manufactures,
17  distributes, dispenses, delivers, or possesses with intent to
18  deliver an anabolic steroid, which anabolic steroid is
19  expressly intended for and lawfully allowed to be administered
20  through implants to livestock or other nonhuman species, and
21  which is approved by the Secretary of Health and Human
22  Services for such administration, and which the person intends
23  to administer or have administered through such implants,
24  shall not be considered to be in unauthorized possession or to
25  unlawfully manufacture, distribute, dispense, deliver, or
26  possess with intent to deliver such anabolic steroid for

 

 

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1  purposes of this Act.
2  (d) "Administration" means the Drug Enforcement
3  Administration, United States Department of Justice, or its
4  successor agency.
5  (d-5) "Clinical Director, Prescription Monitoring Program"
6  means a Department of Human Services administrative employee
7  licensed to either prescribe or dispense controlled substances
8  who shall run the clinical aspects of the Department of Human
9  Services Prescription Monitoring Program and its Prescription
10  Information Library.
11  (d-10) "Compounding" means the preparation and mixing of
12  components, excluding flavorings, (1) as the result of a
13  prescriber's prescription drug order or initiative based on
14  the prescriber-patient-pharmacist relationship in the course
15  of professional practice or (2) for the purpose of, or
16  incident to, research, teaching, or chemical analysis and not
17  for sale or dispensing. "Compounding" includes the preparation
18  of drugs or devices in anticipation of receiving prescription
19  drug orders based on routine, regularly observed dispensing
20  patterns. Commercially available products may be compounded
21  for dispensing to individual patients only if both of the
22  following conditions are met: (i) the commercial product is
23  not reasonably available from normal distribution channels in
24  a timely manner to meet the patient's needs and (ii) the
25  prescribing practitioner has requested that the drug be
26  compounded.

 

 

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1  (e) "Control" means to add a drug or other substance, or
2  immediate precursor, to a Schedule whether by transfer from
3  another Schedule or otherwise.
4  (f) "Controlled Substance" means (i) a drug, substance,
5  immediate precursor, or synthetic drug in the Schedules of
6  Article II of this Act or (ii) a drug or other substance, or
7  immediate precursor, designated as a controlled substance by
8  the Department through administrative rule. The term does not
9  include distilled spirits, wine, malt beverages, or tobacco,
10  as those terms are defined or used in the Liquor Control Act of
11  1934 and the Tobacco Products Tax Act of 1995.
12  (f-5) "Controlled substance analog" means a substance:
13  (1) the chemical structure of which is substantially
14  similar to the chemical structure of a controlled
15  substance in Schedule I or II;
16  (2) which has a stimulant, depressant, or
17  hallucinogenic effect on the central nervous system that
18  is substantially similar to or greater than the stimulant,
19  depressant, or hallucinogenic effect on the central
20  nervous system of a controlled substance in Schedule I or
21  II; or
22  (3) with respect to a particular person, which such
23  person represents or intends to have a stimulant,
24  depressant, or hallucinogenic effect on the central
25  nervous system that is substantially similar to or greater
26  than the stimulant, depressant, or hallucinogenic effect

 

 

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1  on the central nervous system of a controlled substance in
2  Schedule I or II.
3  (g) "Counterfeit substance" means a controlled substance,
4  which, or the container or labeling of which, without
5  authorization bears the trademark, trade name, or other
6  identifying mark, imprint, number or device, or any likeness
7  thereof, of a manufacturer, distributor, or dispenser other
8  than the person who in fact manufactured, distributed, or
9  dispensed the substance.
10  (h) "Deliver" or "delivery" means the actual, constructive
11  or attempted transfer of possession of a controlled substance,
12  with or without consideration, whether or not there is an
13  agency relationship. "Deliver" or "delivery" does not include
14  the donation of drugs to the extent permitted under the
15  Illinois Drug Reuse Opportunity Program Act.
16  (i) "Department" means the Illinois Department of Human
17  Services (as successor to the Department of Alcoholism and
18  Substance Abuse) or its successor agency.
19  (j) (Blank).
20  (k) "Department of Corrections" means the Department of
21  Corrections of the State of Illinois or its successor agency.
22  (l) "Department of Financial and Professional Regulation"
23  means the Department of Financial and Professional Regulation
24  of the State of Illinois or its successor agency.
25  (m) "Depressant" means any drug that (i) causes an overall
26  depression of central nervous system functions, (ii) causes

 

 

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1  impaired consciousness and awareness, and (iii) can be
2  habit-forming or lead to a substance abuse problem, including,
3  but not limited to, alcohol, cannabis and its active
4  principles and their analogs, benzodiazepines and their
5  analogs, barbiturates and their analogs, opioids (natural and
6  synthetic) and their analogs, and chloral hydrate and similar
7  sedative hypnotics.
8  (n) (Blank).
9  (o) "Director" means the Director of the Illinois State
10  Police or his or her designated agents.
11  (p) "Dispense" means to deliver a controlled substance to
12  an ultimate user or research subject by or pursuant to the
13  lawful order of a prescriber, including the prescribing,
14  administering, packaging, labeling, or compounding necessary
15  to prepare the substance for that delivery.
16  (q) "Dispenser" means a practitioner who dispenses.
17  (r) "Distribute" means to deliver, other than by
18  administering or dispensing, a controlled substance.
19  (s) "Distributor" means a person who distributes.
20  (t) "Drug" means (1) substances recognized as drugs in the
21  official United States Pharmacopoeia, Official Homeopathic
22  Pharmacopoeia of the United States, or official National
23  Formulary, or any supplement to any of them; (2) substances
24  intended for use in diagnosis, cure, mitigation, treatment, or
25  prevention of disease in man or animals; (3) substances (other
26  than food) intended to affect the structure of any function of

 

 

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1  the body of man or animals and (4) substances intended for use
2  as a component of any article specified in clause (1), (2), or
3  (3) of this subsection. It does not include devices or their
4  components, parts, or accessories.
5  (t-3) "Electronic health record" or "EHR" means an
6  electronic record of health-related information on an
7  individual that is created, gathered, managed, and consulted
8  by authorized health care clinicians and staff.
9  (t-3.5) "Electronic health record system" or "EHR system"
10  means any computer-based system or combination of federally
11  certified Health IT Modules (defined at 42 CFR 170.102 or its
12  successor) used as a repository for electronic health records
13  and accessed or updated by a prescriber or authorized
14  surrogate in the ordinary course of his or her medical
15  practice. For purposes of connecting to the Prescription
16  Information Library maintained by the Bureau of Pharmacy and
17  Clinical Support Systems or its successor, an EHR system may
18  connect to the Prescription Information Library directly or
19  through all or part of a computer program or system that is a
20  federally certified Health IT Module maintained by a third
21  party and used by the EHR system to secure access to the
22  database.
23  (t-4) "Emergency medical services personnel" has the
24  meaning ascribed to it in the Emergency Medical Services (EMS)
25  Systems Act.
26  (t-5) "Euthanasia agency" means an entity certified by the

 

 

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1  Department of Financial and Professional Regulation for the
2  purpose of animal euthanasia that holds an animal control
3  facility license or animal shelter license under the Animal
4  Welfare Act. A euthanasia agency is authorized to purchase,
5  store, possess, and utilize Schedule II nonnarcotic and
6  Schedule III nonnarcotic drugs for the sole purpose of animal
7  euthanasia.
8  (t-10) "Euthanasia drugs" means Schedule II or Schedule
9  III substances (nonnarcotic controlled substances) that are
10  used by a euthanasia agency for the purpose of animal
11  euthanasia.
12  (u) "Good faith" means the prescribing or dispensing of a
13  controlled substance by a practitioner in the regular course
14  of professional treatment to or for any person who is under his
15  or her treatment for a pathology or condition other than that
16  individual's physical or psychological dependence upon or
17  addiction to a controlled substance, except as provided
18  herein: and application of the term to a pharmacist shall mean
19  the dispensing of a controlled substance pursuant to the
20  prescriber's order which in the professional judgment of the
21  pharmacist is lawful. The pharmacist shall be guided by
22  accepted professional standards, including, but not limited
23  to, the following, in making the judgment:
24  (1) lack of consistency of prescriber-patient
25  relationship,
26  (2) frequency of prescriptions for same drug by one

 

 

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1  prescriber for large numbers of patients,
2  (3) quantities beyond those normally prescribed,
3  (4) unusual dosages (recognizing that there may be
4  clinical circumstances where more or less than the usual
5  dose may be used legitimately),
6  (5) unusual geographic distances between patient,
7  pharmacist and prescriber,
8  (6) consistent prescribing of habit-forming drugs.
9  (u-0.5) "Hallucinogen" means a drug that causes markedly
10  altered sensory perception leading to hallucinations of any
11  type.
12  (u-1) "Home infusion services" means services provided by
13  a pharmacy in compounding solutions for direct administration
14  to a patient in a private residence, long-term care facility,
15  or hospice setting by means of parenteral, intravenous,
16  intramuscular, subcutaneous, or intraspinal infusion.
17  (u-5) "Illinois State Police" means the Illinois State
18  Police or its successor agency.
19  (v) "Immediate precursor" means a substance:
20  (1) which the Department has found to be and by rule
21  designated as being a principal compound used, or produced
22  primarily for use, in the manufacture of a controlled
23  substance;
24  (2) which is an immediate chemical intermediary used
25  or likely to be used in the manufacture of such controlled
26  substance; and

 

 

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1  (3) the control of which is necessary to prevent,
2  curtail or limit the manufacture of such controlled
3  substance.
4  (w) "Instructional activities" means the acts of teaching,
5  educating or instructing by practitioners using controlled
6  substances within educational facilities approved by the State
7  Board of Education or its successor agency.
8  (x) "Local authorities" means a duly organized State,
9  County or Municipal peace unit or police force.
10  (y) "Look-alike substance" means a substance, other than a
11  controlled substance which (1) by overall dosage unit
12  appearance, including shape, color, size, markings or lack
13  thereof, taste, consistency, or any other identifying physical
14  characteristic of the substance, would lead a reasonable
15  person to believe that the substance is a controlled
16  substance, or (2) is expressly or impliedly represented to be
17  a controlled substance or is distributed under circumstances
18  which would lead a reasonable person to believe that the
19  substance is a controlled substance. For the purpose of
20  determining whether the representations made or the
21  circumstances of the distribution would lead a reasonable
22  person to believe the substance to be a controlled substance
23  under this clause (2) of subsection (y), the court or other
24  authority may consider the following factors in addition to
25  any other factor that may be relevant:
26  (a) statements made by the owner or person in control

 

 

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1  of the substance concerning its nature, use or effect;
2  (b) statements made to the buyer or recipient that the
3  substance may be resold for profit;
4  (c) whether the substance is packaged in a manner
5  normally used for the illegal distribution of controlled
6  substances;
7  (d) whether the distribution or attempted distribution
8  included an exchange of or demand for money or other
9  property as consideration, and whether the amount of the
10  consideration was substantially greater than the
11  reasonable retail market value of the substance.
12  Clause (1) of this subsection (y) shall not apply to a
13  noncontrolled substance in its finished dosage form that was
14  initially introduced into commerce prior to the initial
15  introduction into commerce of a controlled substance in its
16  finished dosage form which it may substantially resemble.
17  Nothing in this subsection (y) prohibits the dispensing or
18  distributing of noncontrolled substances by persons authorized
19  to dispense and distribute controlled substances under this
20  Act, provided that such action would be deemed to be carried
21  out in good faith under subsection (u) if the substances
22  involved were controlled substances.
23  Nothing in this subsection (y) or in this Act prohibits
24  the manufacture, preparation, propagation, compounding,
25  processing, packaging, advertising or distribution of a drug
26  or drugs by any person registered pursuant to Section 510 of

 

 

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1  the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 360).
2  (y-1) "Mail-order pharmacy" means a pharmacy that is
3  located in a state of the United States that delivers,
4  dispenses or distributes, through the United States Postal
5  Service or other common carrier, to Illinois residents, any
6  substance which requires a prescription.
7  (z) "Manufacture" means the production, preparation,
8  propagation, compounding, conversion or processing of a
9  controlled substance other than methamphetamine, either
10  directly or indirectly, by extraction from substances of
11  natural origin, or independently by means of chemical
12  synthesis, or by a combination of extraction and chemical
13  synthesis, and includes any packaging or repackaging of the
14  substance or labeling of its container, except that this term
15  does not include:
16  (1) by an ultimate user, the preparation or
17  compounding of a controlled substance for his or her own
18  use;
19  (2) by a practitioner, or his or her authorized agent
20  under his or her supervision, the preparation,
21  compounding, packaging, or labeling of a controlled
22  substance:
23  (a) as an incident to his or her administering or
24  dispensing of a controlled substance in the course of
25  his or her professional practice; or
26  (b) as an incident to lawful research, teaching or

 

 

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1  chemical analysis and not for sale; or
2  (3) the packaging, repackaging, or labeling of drugs
3  only to the extent permitted under the Illinois Drug Reuse
4  Opportunity Program Act.
5  (z-1) (Blank).
6  (z-5) "Medication shopping" means the conduct prohibited
7  under subsection (a) of Section 314.5 of this Act.
8  (z-10) "Mid-level practitioner" means (i) a physician
9  assistant who has been delegated authority to prescribe
10  through a written delegation of authority by a physician
11  licensed to practice medicine in all of its branches, in
12  accordance with Section 7.5 of the Physician Assistant
13  Practice Act of 1987, (ii) an advanced practice registered
14  nurse who has been delegated authority to prescribe through a
15  written delegation of authority by a physician licensed to
16  practice medicine in all of its branches or by a podiatric
17  physician, in accordance with Section 65-40 of the Nurse
18  Practice Act, (iii) an advanced practice registered nurse
19  certified as a nurse practitioner, nurse midwife, or clinical
20  nurse specialist who has been granted authority to prescribe
21  by a hospital affiliate in accordance with Section 65-45 of
22  the Nurse Practice Act, (iv) an animal euthanasia agency, or
23  (v) a prescribing psychologist.
24  (aa) "Narcotic drug" means any of the following, whether
25  produced directly or indirectly by extraction from substances
26  of vegetable origin, or independently by means of chemical

 

 

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1  synthesis, or by a combination of extraction and chemical
2  synthesis:
3  (1) opium, opiates, derivatives of opium and opiates,
4  including their isomers, esters, ethers, salts, and salts
5  of isomers, esters, and ethers, whenever the existence of
6  such isomers, esters, ethers, and salts is possible within
7  the specific chemical designation; however the term
8  "narcotic drug" does not include the isoquinoline
9  alkaloids of opium;
10  (2) (blank);
11  (3) opium poppy and poppy straw;
12  (4) coca leaves, except coca leaves and extracts of
13  coca leaves from which substantially all of the cocaine
14  and ecgonine, and their isomers, derivatives and salts,
15  have been removed;
16  (5) cocaine, its salts, optical and geometric isomers,
17  and salts of isomers;
18  (6) ecgonine, its derivatives, their salts, isomers,
19  and salts of isomers;
20  (7) any compound, mixture, or preparation which
21  contains any quantity of any of the substances referred to
22  in subparagraphs (1) through (6).
23  (bb) "Nurse" means a registered nurse licensed under the
24  Nurse Practice Act.
25  (cc) (Blank).
26  (dd) "Opiate" means any substance having an addiction

 

 

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1  forming or addiction sustaining liability similar to morphine
2  or being capable of conversion into a drug having addiction
3  forming or addiction sustaining liability.
4  (ee) "Opium poppy" means the plant of the species Papaver
5  somniferum L., except its seeds.
6  (ee-5) "Oral dosage" means a tablet, capsule, elixir, or
7  solution or other liquid form of medication intended for
8  administration by mouth, but the term does not include a form
9  of medication intended for buccal, sublingual, or transmucosal
10  administration.
11  (ff) "Parole and Pardon Board" means the Parole and Pardon
12  Board of the State of Illinois or its successor agency.
13  (gg) "Person" means any individual, corporation,
14  mail-order pharmacy, government or governmental subdivision or
15  agency, business trust, estate, trust, partnership or
16  association, or any other entity.
17  (hh) "Pharmacist" means any person who holds a license or
18  certificate of registration as a registered pharmacist, a
19  local registered pharmacist or a registered assistant
20  pharmacist under the Pharmacy Practice Act.
21  (ii) "Pharmacy" means any store, ship or other place in
22  which pharmacy is authorized to be practiced under the
23  Pharmacy Practice Act.
24  (ii-5) "Pharmacy shopping" means the conduct prohibited
25  under subsection (b) of Section 314.5 of this Act.
26  (ii-10) "Physician" (except when the context otherwise

 

 

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1  requires) means a person licensed to practice medicine in all
2  of its branches.
3  (jj) "Poppy straw" means all parts, except the seeds, of
4  the opium poppy, after mowing.
5  (kk) "Practitioner" means a physician licensed to practice
6  medicine in all its branches, dentist, optometrist, podiatric
7  physician, veterinarian, scientific investigator, pharmacist,
8  physician assistant, advanced practice registered nurse,
9  licensed practical nurse, registered nurse, emergency medical
10  services personnel, hospital, laboratory, or pharmacy, or
11  other person licensed, registered, or otherwise lawfully
12  permitted by the United States or this State to distribute,
13  dispense, conduct research with respect to, administer or use
14  in teaching or chemical analysis, a controlled substance in
15  the course of professional practice or research.
16  (ll) "Pre-printed prescription" means a written
17  prescription upon which the designated drug has been indicated
18  prior to the time of issuance; the term does not mean a written
19  prescription that is individually generated by machine or
20  computer in the prescriber's office.
21  (mm) "Prescriber" means a physician licensed to practice
22  medicine in all its branches, dentist, optometrist,
23  prescribing psychologist licensed under Section 4.2 of the
24  Clinical Psychologist Licensing Act with prescriptive
25  authority delegated under Section 4.3 of the Clinical
26  Psychologist Licensing Act, podiatric physician, or

 

 

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1  veterinarian who issues a prescription, a physician assistant
2  who issues a prescription for a controlled substance in
3  accordance with Section 303.05, a written delegation, and a
4  written collaborative agreement required under Section 7.5 of
5  the Physician Assistant Practice Act of 1987, an advanced
6  practice registered nurse with prescriptive authority
7  delegated under Section 65-40 of the Nurse Practice Act and in
8  accordance with Section 303.05, a written delegation, and a
9  written collaborative agreement under Section 65-35 of the
10  Nurse Practice Act, an advanced practice registered nurse
11  certified as a nurse practitioner, nurse midwife, or clinical
12  nurse specialist who has been granted authority to prescribe
13  by a hospital affiliate in accordance with Section 65-45 of
14  the Nurse Practice Act and in accordance with Section 303.05,
15  or an advanced practice registered nurse certified as a nurse
16  practitioner, nurse midwife, or clinical nurse specialist who
17  has full practice authority pursuant to Section 65-43 of the
18  Nurse Practice Act.
19  (nn) "Prescription" means a written, facsimile, or oral
20  order, or an electronic order that complies with applicable
21  federal requirements, of a physician licensed to practice
22  medicine in all its branches, dentist, podiatric physician or
23  veterinarian for any controlled substance, of an optometrist
24  in accordance with Section 15.1 of the Illinois Optometric
25  Practice Act of 1987, of a prescribing psychologist licensed
26  under Section 4.2 of the Clinical Psychologist Licensing Act

 

 

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1  with prescriptive authority delegated under Section 4.3 of the
2  Clinical Psychologist Licensing Act, of a physician assistant
3  for a controlled substance in accordance with Section 303.05,
4  a written delegation, and a written collaborative agreement
5  required under Section 7.5 of the Physician Assistant Practice
6  Act of 1987, of an advanced practice registered nurse with
7  prescriptive authority delegated under Section 65-40 of the
8  Nurse Practice Act who issues a prescription for a controlled
9  substance in accordance with Section 303.05, a written
10  delegation, and a written collaborative agreement under
11  Section 65-35 of the Nurse Practice Act, of an advanced
12  practice registered nurse certified as a nurse practitioner,
13  nurse midwife, or clinical nurse specialist who has been
14  granted authority to prescribe by a hospital affiliate in
15  accordance with Section 65-45 of the Nurse Practice Act and in
16  accordance with Section 303.05 when required by law, or of an
17  advanced practice registered nurse certified as a nurse
18  practitioner, nurse midwife, or clinical nurse specialist who
19  has full practice authority pursuant to Section 65-43 of the
20  Nurse Practice Act.
21  (nn-5) "Prescription Information Library" (PIL) means an
22  electronic library that contains reported controlled substance
23  data.
24  (nn-10) "Prescription Monitoring Program" (PMP) means the
25  entity that collects, tracks, and stores reported data on
26  controlled substances and select drugs pursuant to Section

 

 

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1  316.
2  (oo) "Production" or "produce" means manufacture,
3  planting, cultivating, growing, or harvesting of a controlled
4  substance other than methamphetamine.
5  (pp) "Registrant" means every person who is required to
6  register under Section 302 of this Act.
7  (qq) "Registry number" means the number assigned to each
8  person authorized to handle controlled substances under the
9  laws of the United States and of this State.
10  (qq-5) "Secretary" means, as the context requires, either
11  the Secretary of the Department or the Secretary of the
12  Department of Financial and Professional Regulation, and the
13  Secretary's designated agents.
14  (rr) "State" includes the State of Illinois and any state,
15  district, commonwealth, territory, insular possession thereof,
16  and any area subject to the legal authority of the United
17  States of America.
18  (rr-5) "Stimulant" means any drug that (i) causes an
19  overall excitation of central nervous system functions, (ii)
20  causes impaired consciousness and awareness, and (iii) can be
21  habit-forming or lead to a substance abuse problem, including,
22  but not limited to, amphetamines and their analogs,
23  methylphenidate and its analogs, cocaine, and phencyclidine
24  and its analogs.
25  (rr-10) "Synthetic drug" includes, but is not limited to,
26  any synthetic cannabinoids or piperazines or any synthetic

 

 

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1  cathinones as provided for in Schedule I.
2  (ss) "Ultimate user" means a person who lawfully possesses
3  a controlled substance for his or her own use or for the use of
4  a member of his or her household or for administering to an
5  animal owned by him or her or by a member of his or her
6  household.
7  (Source: P.A. 101-666, eff. 1-1-22; 102-389, eff. 1-1-22;
8  102-538, eff. 8-20-21; 102-813, eff. 5-13-22.)
9  (720 ILCS 570/303.05)
10  Sec. 303.05. Mid-level practitioner registration.
11  (a) The Department of Financial and Professional
12  Regulation shall register licensed physician assistants,
13  licensed advanced practice registered nurses, and prescribing
14  psychologists licensed under Section 4.2 of the Clinical
15  Psychologist Licensing Act to prescribe and dispense
16  controlled substances under Section 303 and euthanasia
17  agencies to purchase, store, or administer animal euthanasia
18  drugs under the following circumstances:
19  (1) with respect to physician assistants,
20  (A) the physician assistant has been delegated
21  written authority to prescribe any Schedule III
22  through V controlled substances by a physician
23  licensed to practice medicine in all its branches in
24  accordance with Section 7.5 of the Physician Assistant
25  Practice Act of 1987; and the physician assistant has

 

 

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1  completed the appropriate application forms and has
2  paid the required fees as set by rule; or
3  (B) the physician assistant has been delegated
4  authority by a collaborating physician licensed to
5  practice medicine in all its branches to prescribe or
6  dispense Schedule II controlled substances through a
7  written delegation of authority and under the
8  following conditions:
9  (i) Specific Schedule II controlled substances
10  by oral dosage or topical or transdermal
11  application may be delegated, provided that the
12  delegated Schedule II controlled substances are
13  routinely prescribed by the collaborating
14  physician. This delegation must identify the
15  specific Schedule II controlled substances by
16  either brand name or generic name. Schedule II
17  controlled substances to be delivered by injection
18  or other route of administration may not be
19  delegated;
20  (ii) any delegation must be of controlled
21  substances prescribed by the collaborating
22  physician;
23  (iii) all prescriptions must be limited to no
24  more than a 30-day supply, with any continuation
25  authorized only after prior approval of the
26  collaborating physician;

 

 

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1  (iv) the physician assistant must discuss the
2  condition of any patients for whom a controlled
3  substance is prescribed monthly with the
4  delegating physician;
5  (A) (v) the physician assistant must have
6  completed the appropriate application forms and paid
7  the required fees as set by rule;
8  (B) (vi) the physician assistant must provide
9  evidence of satisfactory completion of 45 contact
10  hours in pharmacology from any physician assistant
11  program accredited by the Accreditation Review
12  Commission on Education for the Physician Assistant
13  (ARC-PA), or its predecessor agency, for any new
14  license issued with Schedule II authority after the
15  effective date of this amendatory Act of the 97th
16  General Assembly; and
17  (C) (vii) the physician assistant must annually
18  complete at least 5 hours of continuing education in
19  pharmacology;
20  (2) with respect to advanced practice registered
21  nurses who do not meet the requirements of Section 65-43
22  of the Nurse Practice Act,
23  (A) the advanced practice registered nurse has
24  been delegated authority to prescribe any Schedule III
25  through V controlled substances by a collaborating
26  physician licensed to practice medicine in all its

 

 

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1  branches or a collaborating podiatric physician in
2  accordance with Section 65-40 of the Nurse Practice
3  Act. The advanced practice registered nurse has
4  completed the appropriate application forms and has
5  paid the required fees as set by rule; or
6  (B) the advanced practice registered nurse has
7  been delegated authority by a collaborating physician
8  licensed to practice medicine in all its branches to
9  prescribe or dispense Schedule II controlled
10  substances through a written delegation of authority
11  and under the following conditions:
12  (i) specific Schedule II controlled substances
13  by oral dosage or topical or transdermal
14  application may be delegated, provided that the
15  delegated Schedule II controlled substances are
16  routinely prescribed by the collaborating
17  physician. This delegation must identify the
18  specific Schedule II controlled substances by
19  either brand name or generic name. Schedule II
20  controlled substances to be delivered by injection
21  or other route of administration may not be
22  delegated;
23  (ii) any delegation must be of controlled
24  substances prescribed by the collaborating
25  physician;
26  (iii) all prescriptions must be limited to no

 

 

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1  more than a 30-day supply, with any continuation
2  authorized only after prior approval of the
3  collaborating physician;
4  (iv) the advanced practice registered nurse
5  must discuss the condition of any patients for
6  whom a controlled substance is prescribed monthly
7  with the delegating physician or in the course of
8  review as required by Section 65-40 of the Nurse
9  Practice Act;
10  (v) the advanced practice registered nurse
11  must have completed the appropriate application
12  forms and paid the required fees as set by rule;
13  (vi) the advanced practice registered nurse
14  must provide evidence of satisfactory completion
15  of at least 45 graduate contact hours in
16  pharmacology for any new license issued with
17  Schedule II authority after the effective date of
18  this amendatory Act of the 97th General Assembly;
19  and
20  (vii) the advanced practice registered nurse
21  must annually complete 5 hours of continuing
22  education in pharmacology;
23  (2.5) with respect to advanced practice registered
24  nurses certified as nurse practitioners, nurse midwives,
25  or clinical nurse specialists who do not meet the
26  requirements of Section 65-43 of the Nurse Practice Act

 

 

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1  practicing in a hospital affiliate,
2  (A) the advanced practice registered nurse
3  certified as a nurse practitioner, nurse midwife, or
4  clinical nurse specialist has been privileged to
5  prescribe any Schedule II through V controlled
6  substances by the hospital affiliate upon the
7  recommendation of the appropriate physician committee
8  of the hospital affiliate in accordance with Section
9  65-45 of the Nurse Practice Act, has completed the
10  appropriate application forms, and has paid the
11  required fees as set by rule; and
12  (B) an advanced practice registered nurse
13  certified as a nurse practitioner, nurse midwife, or
14  clinical nurse specialist has been privileged to
15  prescribe any Schedule II controlled substances by the
16  hospital affiliate upon the recommendation of the
17  appropriate physician committee of the hospital
18  affiliate, then the following conditions must be met:
19  (i) specific Schedule II controlled substances
20  by oral dosage or topical or transdermal
21  application may be designated, provided that the
22  designated Schedule II controlled substances are
23  routinely prescribed by advanced practice
24  registered nurses in their area of certification;
25  the privileging documents must identify the
26  specific Schedule II controlled substances by

 

 

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1  either brand name or generic name; privileges to
2  prescribe or dispense Schedule II controlled
3  substances to be delivered by injection or other
4  route of administration may not be granted;
5  (ii) any privileges must be controlled
6  substances limited to the practice of the advanced
7  practice registered nurse;
8  (iii) any prescription must be limited to no
9  more than a 30-day supply;
10  (iv) the advanced practice registered nurse
11  must discuss the condition of any patients for
12  whom a controlled substance is prescribed monthly
13  with the appropriate physician committee of the
14  hospital affiliate or its physician designee; and
15  (v) the advanced practice registered nurse
16  must meet the education requirements of this
17  Section;
18  (3) with respect to animal euthanasia agencies, the
19  euthanasia agency has obtained a license from the
20  Department of Financial and Professional Regulation and
21  obtained a registration number from the Department; or
22  (4) with respect to prescribing psychologists, the
23  prescribing psychologist has been delegated authority to
24  prescribe any nonnarcotic Schedule III through V
25  controlled substances by a collaborating physician
26  licensed to practice medicine in all its branches in

 

 

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1  accordance with Section 4.3 of the Clinical Psychologist
2  Licensing Act, and the prescribing psychologist has
3  completed the appropriate application forms and has paid
4  the required fees as set by rule.
5  (b) The mid-level practitioner shall only be licensed to
6  prescribe those schedules of controlled substances for which a
7  licensed physician has delegated prescriptive authority,
8  except that an animal euthanasia agency does not have any
9  prescriptive authority and a physician assistant shall have
10  prescriptive authority in accordance with the Physician
11  Assistant Practice Act of 1987 without delegation by a
12  physician. An A physician assistant and an advanced practice
13  registered nurse is are prohibited from prescribing
14  medications and controlled substances not set forth in the
15  required written delegation of authority or as authorized by
16  their practice Act.
17  (c) Upon completion of all registration requirements,
18  physician assistants, advanced practice registered nurses, and
19  animal euthanasia agencies may be issued a mid-level
20  practitioner controlled substances license for Illinois.
21  (d) A collaborating physician may, but is not required to,
22  delegate prescriptive authority to an advanced practice
23  registered nurse as part of a written collaborative agreement,
24  and the delegation of prescriptive authority shall conform to
25  the requirements of Section 65-40 of the Nurse Practice Act.
26  (e) (Blank). A collaborating physician may, but is not

 

 

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1  required to, delegate prescriptive authority to a physician
2  assistant as part of a written collaborative agreement, and
3  the delegation of prescriptive authority shall conform to the
4  requirements of Section 7.5 of the Physician Assistant
5  Practice Act of 1987.
6  (f) Nothing in this Section shall be construed to prohibit
7  generic substitution.
8  (Source: P.A. 99-173, eff. 7-29-15; 100-453, eff. 8-25-17;
9  100-513, eff. 1-1-18; 100-863, eff. 8-14-18.)

 

 

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