H.B. 230 LEGISLATIVE GENERAL COUNSEL 6 Approved for Filing: C. Williams 6 6 01-17-23 2:26 PM 6 H.B. 230 1 CENTER FOR MEDI CAL CANNABIS RESEARCH 2 2023 GENERAL SESSION 3 STATE OF UTAH 4 Chief Sponsor: Jennifer Dailey-Provost 5 Senate Sponsor: ____________ 6 7LONG TITLE 8General Description: 9 This bill creates the Center for Medical Cannabis Research. 10Highlighted Provisions: 11 This bill: 12 <defines terms; 13 <abolishes the Cannabis Research Review Board; 14 <creates the Center for Medical Cannabis Research (center) within the University of 15Utah; and 16 <establishes the center's duties. 17Money Appropriated in this Bill: 18 None 19Other Special Clauses: 20 None 21Utah Code Sections Affected: 22AMENDS: 23 4-41a-102, as last amended by Laws of Utah 2022, Chapters 290, 452 24 26-61a-102, as last amended by Laws of Utah 2022, Chapters 290, 452 25 26-61a-105, as last amended by Laws of Utah 2022, Chapter 452 26 26-61a-201, as last amended by Laws of Utah 2022, Chapters 198, 290 and 452 27 26-61a-703, as last amended by Laws of Utah 2022, Chapter 97 *HB0230* H.B. 230 01-17-23 2:26 PM - 2 - 28ENACTS: 29 53B-17-1401, Utah Code Annotated 1953 30 53B-17-1402, Utah Code Annotated 1953 31REPEALS: 32 26-61-101, as enacted by Laws of Utah 2017, Chapter 398 33 26-61-102, as last amended by Laws of Utah 2022, Chapter 452 34 26-61-103, as enacted by Laws of Utah 2017, Chapter 398 35 26-61-201, as last amended by Laws of Utah 2022, Chapter 452 36 26-61-202, as last amended by Laws of Utah 2022, Chapter 415 37 38Be it enacted by the Legislature of the state of Utah: 39 Section 1. Section 4-41a-102 is amended to read: 40 4-41a-102. Definitions. 41 As used in this chapter: 42 (1) "Adulterant" means any poisonous or deleterious substance in a quantity that may 43be injurious to health, including: 44 (a) pesticides; 45 (b) heavy metals; 46 (c) solvents; 47 (d) microbial life; 48 (e) toxins; or 49 (f) foreign matter. 50 [(2) " Cannabis Research Review Board" means the Cannabis Research Review Board 51created in Section 26-61-201.] 52 [(3)] (2) "Cannabis" means the same as that term is defined in Section 26-61a-102. 53 [(4)] (3) "Cannabis concentrate" means: 54 (a) the product of any chemical or physical process applied to naturally occurring 55biomass that concentrates or isolates the cannabinoids contained in the biomass; and 56 (b) any amount of a natural, derivative, or synthetic cannabinoid in the synthetic 57cannabinoid's purified state. 58 [(5)] (4) "Cannabis cultivation byproduct" means any portion of a cannabis plant that is 01-17-23 2:26 PM H.B. 230 - 3 - 59not intended to be sold as a cannabis plant product. 60 [(6)] (5) "Cannabis cultivation facility" means a person that: 61 (a) possesses cannabis; 62 (b) grows or intends to grow cannabis; and 63 (c) sells or intends to sell cannabis to a cannabis cultivation facility, a cannabis 64processing facility, or a medical cannabis research licensee. 65 [(7)] (6) "Cannabis cultivation facility agent" means an individual who: 66 (a) is an employee of a cannabis cultivation facility; and 67 (b) holds a valid cannabis production establishment agent registration card. 68 [(8)] (7) "Cannabis derivative product" means a product made using cannabis 69concentrate. 70 [(9)] (8) "Cannabis plant product" means any portion of a cannabis plant intended to be 71sold in a form that is recognizable as a portion of a cannabis plant. 72 [(10)] (9) "Cannabis processing facility" means a person that: 73 (a) acquires or intends to acquire cannabis from a cannabis production establishment; 74 (b) possesses cannabis with the intent to manufacture a cannabis product; 75 (c) manufactures or intends to manufacture a cannabis product from unprocessed 76cannabis or a cannabis extract; and 77 (d) sells or intends to sell a cannabis product to a medical cannabis pharmacy or a 78medical cannabis research licensee. 79 [(11)] (10) "Cannabis processing facility agent" means an individual who: 80 (a) is an employee of a cannabis processing facility; and 81 (b) holds a valid cannabis production establishment agent registration card. 82 [(12)] (11) "Cannabis product" means the same as that term is defined in Section 8326-61a-102. 84 [(13)] (12) "Cannabis production establishment" means a cannabis cultivation facility, 85a cannabis processing facility, or an independent cannabis testing laboratory. 86 [(14)] (13) "Cannabis production establishment agent" means a cannabis cultivation 87facility agent, a cannabis processing facility agent, or an independent cannabis testing 88laboratory agent. 89 [(15)] (14) "Cannabis production establishment agent registration card" means a H.B. 230 01-17-23 2:26 PM - 4 - 90registration card that the department issues that: 91 (a) authorizes an individual to act as a cannabis production establishment agent; and 92 (b) designates the type of cannabis production establishment for which an individual is 93authorized to act as an agent. 94 [(16)] (15) "Community location" means a public or private elementary or secondary 95school, a church, a public library, a public playground, or a public park. 96 [(17)] (16) "Cultivation space" means, quantified in square feet, the horizontal area in 97which a cannabis cultivation facility cultivates cannabis, including each level of horizontal area 98if the cannabis cultivation facility hangs, suspends, stacks, or otherwise positions plants above 99other plants in multiple levels. 100 [(18)] (17) "Department" means the Department of Agriculture and Food. 101 [(19)] (18) "Derivative cannabinoid" means any cannabinoid that has been intentionally 102created using a process to convert a naturally occurring cannabinoid into another cannabinoid. 103 [(20)] (19) "Family member" means a parent, step-parent, spouse, child, sibling, 104step-sibling, uncle, aunt, nephew, niece, first cousin, mother-in-law, father-in-law, 105brother-in-law, sister-in-law, son-in-law, daughter-in-law, grandparent, or grandchild. 106 [(21)] (20) (a) "Independent cannabis testing laboratory" means a person that: 107 (i) conducts a chemical or other analysis of cannabis or a cannabis product; or 108 (ii) acquires, possesses, and transports cannabis or a cannabis product with the intent to 109conduct a chemical or other analysis of the cannabis or cannabis product. 110 (b) "Independent cannabis testing laboratory" includes a laboratory that the department 111or a research university operates in accordance with Subsection 4-41a-201(14). 112 [(22)] (21) "Independent cannabis testing laboratory agent" means an individual who: 113 (a) is an employee of an independent cannabis testing laboratory; and 114 (b) holds a valid cannabis production establishment agent registration card. 115 [(23)] (22) "Industrial hemp waste" means: 116 (a) a cannabinoid concentrate; or 117 (b) industrial hemp biomass. 118 [(24)] (23) "Inventory control system" means a system described in Section 4-41a-103. 119 [(25)] (24) "Licensing board" or "board" means the Cannabis Production Establishment 120Licensing Advisory Board created in Section 4-41a-201.1. 01-17-23 2:26 PM H.B. 230 - 5 - 121 [(26)] (25) "Medical cannabis" means the same as that term is defined in Section 12226-61a-102. 123 [(27)] (26) "Medical cannabis card" means the same as that term is defined in Section 12426-61a-102. 125 [(28)] (27) "Medical cannabis pharmacy" means the same as that term is defined in 126Section 26-61a-102. 127 [(29)] (28) "Medical cannabis pharmacy agent" means the same as that term is defined 128in Section 26-61a-102. 129 [(30)] (29) "Medical cannabis research license" means a license that the department 130issues to a research university for the purpose of obtaining and possessing medical cannabis for 131academic research. 132 [(31)] (30) "Medical cannabis research licensee" means a research university that the 133department licenses to obtain and possess medical cannabis for academic research, in 134accordance with Section 4-41a-901. 135 [(32)] (31) "Medical cannabis treatment" means the same as that term is defined in 136Section 26-61a-102. 137 [(33)] (32) "Medicinal dosage form" means the same as that term is defined in Section 13826-61a-102. 139 [(34)] (33) "Qualified medical provider" means the same as that term is defined in 140Section 26-61a-102. 141 [(35)] (34) "Qualified Production Enterprise Fund" means the fund created in Section 1424-41a-104. 143 [(36)] (35) "Recommending medical provider" means the same as that term is defined 144in Section 26-61a-102. 145 [(37)] (36) "Research university" means the same as that term is defined in Section 14653B-7-702 and a private, nonprofit college or university in the state that: 147 (a) is accredited by the Northwest Commission on Colleges and Universities; 148 (b) grants doctoral degrees; and 149 (c) has a laboratory containing or a program researching a schedule I controlled 150substance described in Section 58-37-4. 151 [(38)] (37) "State electronic verification system" means the system described in Section H.B. 230 01-17-23 2:26 PM - 6 - 15226-61a-103. 153 [(39)] (38) "Synthetic cannabinoid" means any cannabinoid that: 154 (a) was chemically synthesized from starting materials other than a naturally occurring 155cannabinoid; and 156 (b) is not a derivative cannabinoid. 157 [(40)] (39) "Tetrahydrocannabinol" or "THC" means the same as that term is defined in 158Section 4-41-102. 159 [(41)] (40) "THC analog" means the same as that term is defined in Section 4-41-102. 160 [(42)] (41) "Total composite tetrahydrocannabinol" means all detectable forms of 161tetrahydrocannabinol. 162 [(43)] (42) "Total tetrahydrocannabinol" or "total THC" means the same as that term is 163defined in Section 4-41-102. 164 Section 2. Section 26-61a-102 is amended to read: 165 26-61a-102. Definitions. 166 As used in this chapter: 167 (1) "Active tetrahydrocannabinol" means THC, any THC analog, and 168tetrahydrocannabinolic acid. 169 [(2) " Cannabis Research Review Board" means the Cannabis Research Review Board 170created in Section 26-61-201.] 171 [(3)] (2) "Cannabis" means marijuana. 172 [(4)] (3) "Cannabis cultivation facility" means the same as that term is defined in 173Section 4-41a-102. 174 [(5)] (4) "Cannabis processing facility" means the same as that term is defined in 175Section 4-41a-102. 176 [(6)] (5) "Cannabis product" means a product that: 177 (a) is intended for human use; and 178 (b) contains cannabis or any tetrahydrocannabinol or THC analog in a total 179concentration of 0.3% or greater on a dry weight basis. 180 [(7)] (6) "Cannabis production establishment" means the same as that term is defined 181in Section 4-41a-102. 182 [(8)] (7) "Cannabis production establishment agent" means the same as that term is 01-17-23 2:26 PM H.B. 230 - 7 - 183defined in Section 4-41a-102. 184 [(9)] (8) "Cannabis production establishment agent registration card" means the same 185as that term is defined in Section 4-41a-102. 186 [(10)] (9) "Community location" means a public or private elementary or secondary 187school, a church, a public library, a public playground, or a public park. 188 [(11)] (10) "Conditional medical cannabis card" means an electronic medical cannabis 189card that the department issues in accordance with Subsection 26-61a-201(1)(b) to allow an 190applicant for a medical cannabis card to access medical cannabis during the department's 191review of the application. 192 [(12)] (11) "Controlled substance database" means the controlled substance database 193created in Section 58-37f-201. 194 [(13)] (12) "Department" means the Department of Health and Human Services. 195 [(14)] (13) "Designated caregiver" means: 196 (a) an individual: 197 (i) whom an individual with a medical cannabis patient card or a medical cannabis 198guardian card designates as the patient's caregiver; and 199 (ii) who registers with the department under Section 26-61a-202; or 200 (b) (i) a facility that an individual designates as a designated caregiver in accordance 201with Subsection 26-61a-202(1)(b); or 202 (ii) an assigned employee of the facility described in Subsection 26-61a-202(1)(b)(ii). 203 [(15)] (14) "Directions of use" means recommended routes of administration for a 204medical cannabis treatment and suggested usage guidelines. 205 [(16)] (15) "Dosing guidelines" means a quantity range and frequency of administration 206for a recommended treatment of medical cannabis. 207 [(17)] (16) "Financial institution" means a bank, trust company, savings institution, or 208credit union, chartered and supervised under state or federal law. 209 [(18)] (17) "Home delivery medical cannabis pharmacy" means a medical cannabis 210pharmacy that the department authorizes, as part of the pharmacy's license, to deliver medical 211cannabis shipments to a medical cannabis cardholder's home address to fulfill electronic orders 212that the state central patient portal facilitates. 213 [(19)] (18) "Institutional review board" means an institutional review board that is H.B. 230 01-17-23 2:26 PM - 8 - 214registered for human subject research by the United States Department of Health and Human 215Services. 216 (19) "Inventory control system" means the system described in Section 4-41a-103. 217 (20) "Legal dosage limit" means an amount that: 218 (a) is sufficient to provide 30 days of treatment based on the dosing guidelines that the 219relevant recommending medical provider or the state central patient portal or pharmacy 220medical provider, in accordance with Subsection 26-61a-502(4) or (5), recommends; and 221 (b) may not exceed: 222 (i) for unprocessed cannabis in a medicinal dosage form, 113 grams by weight; and 223 (ii) for a cannabis product in a medicinal dosage form, a quantity that contains, in total, 224greater than 20 grams of active tetrahydrocannabinol. 225 (21) "Legal use termination date" means a date on the label of a container of 226unprocessed cannabis flower: 227 (a) that is 60 days after the date of purchase of the cannabis; and 228 (b) after which, the cannabis is no longer in a medicinal dosage form outside of the 229primary residence of the relevant medical cannabis patient cardholder. 230 (22) "Limited medical provider" means an individual who: 231 (a) meets the recommending qualifications; and 232 (b) has no more than 15 patients with a valid medical cannabis patient card or 233provisional patient card as a result of the individual's recommendation, in accordance with 234Subsection 26-61a-106(1)(b). 235 (23) "Marijuana" means the same as that term is defined in Section 58-37-2. 236 (24) "Medical cannabis" means cannabis in a medicinal dosage form or a cannabis 237product in a medicinal dosage form. 238 (25) "Medical cannabis card" means a medical cannabis patient card, a medical 239cannabis guardian card, a medical cannabis caregiver card, or a conditional medical cannabis 240card. 241 (26) "Medical cannabis cardholder" means: 242 (a) a holder of a medical cannabis card; or 243 (b) a facility or assigned employee, described in Subsection(14)(b), only: 244 (i) within the scope of the facility's or assigned employee's performance of the role of a 01-17-23 2:26 PM H.B. 230 - 9 - 245medical cannabis patient cardholder's caregiver designation under Subsection 24626-61a-202(1)(b); and 247 (ii) while in possession of documentation that establishes: 248 (A) a caregiver designation described in Subsection 26-61a-202(1)(b); 249 (B) the identity of the individual presenting the documentation; and 250 (C) the relation of the individual presenting the documentation to the caregiver 251designation. 252 (27) "Medical cannabis caregiver card" means an electronic document that a cardholder 253may print or store on an electronic device or a physical card or document that: 254 (a) the department issues to an individual whom a medical cannabis patient cardholder 255or a medical cannabis guardian cardholder designates as a designated caregiver; and 256 (b) is connected to the electronic verification system. 257 (28) "Medical cannabis courier" means a courier that: 258 (a) the department licenses in accordance with Section 26-61a-604; and 259 (b) contracts with a home delivery medical cannabis pharmacy to deliver medical 260cannabis shipments to fulfill electronic orders that the state central patient portal facilitates. 261 (29) "Medical cannabis courier agent" means an individual who: 262 (a) is an employee of a medical cannabis courier; and 263 (b) who holds a valid medical cannabis courier agent registration card. 264 (30) (a) "Medical cannabis device" means a device that an individual uses to ingest or 265inhale cannabis in a medicinal dosage form or a cannabis product in a medicinal dosage form. 266 (b) "Medical cannabis device" does not include a device that: 267 (i) facilitates cannabis combustion; or 268 (ii) an individual uses to ingest substances other than cannabis. 269 (31) "Medical cannabis guardian card" means an electronic document that a cardholder 270may print or store on an electronic device or a physical card or document that: 271 (a) the department issues to the parent or legal guardian of a minor with a qualifying 272condition; and 273 (b) is connected to the electronic verification system. 274 (32) "Medical cannabis patient card" means an electronic document that a cardholder 275may print or store on an electronic device or a physical card or document that: H.B. 230 01-17-23 2:26 PM - 10 - 276 (a) the department issues to an individual with a qualifying condition; and 277 (b) is connected to the electronic verification system. 278 (33) "Medical cannabis pharmacy" means a person that: 279 (a) (i) acquires or intends to acquire medical cannabis or a cannabis product in a 280medicinal dosage form from a cannabis processing facility or another medical cannabis 281pharmacy or a medical cannabis device; or 282 (ii) possesses medical cannabis or a medical cannabis device; and 283 (b) sells or intends to sell medical cannabis or a medical cannabis device to a medical 284cannabis cardholder. 285 (34) "Medical cannabis pharmacy agent" means an individual who: 286 (a) is an employee of a medical cannabis pharmacy; and 287 (b) who holds a valid medical cannabis pharmacy agent registration card. 288 (35) "Medical cannabis pharmacy agent registration card" means a registration card 289issued by the department that authorizes an individual to act as a medical cannabis pharmacy 290agent. 291 (36) "Medical cannabis shipment" means a shipment of medical cannabis or a medical 292cannabis product that a home delivery medical cannabis pharmacy or a medical cannabis 293courier delivers to a medical cannabis cardholder's home address to fulfill an electronic medical 294cannabis order that the state central patient portal facilitates. 295 (37) "Medical cannabis treatment" means cannabis in a medicinal dosage form, a 296cannabis product in a medicinal dosage form, or a medical cannabis device. 297 (38) (a) "Medicinal dosage form" means: 298 (i) for processed medical cannabis or a medical cannabis product, the following with a 299specific and consistent cannabinoid content: 300 (A) a tablet; 301 (B) a capsule; 302 (C) a concentrated liquid or viscous oil; 303 (D) a liquid suspension that, after December 1, 2022, does not exceed 30 ml; 304 (E) a topical preparation; 305 (F) a transdermal preparation; 306 (G) a sublingual preparation; 01-17-23 2:26 PM H.B. 230 - 11 - 307 (H) a gelatinous cube, gelatinous rectangular cuboid, or lozenge in a cube or 308rectangular cuboid shape; 309 (I) a resin or wax; or 310 (J) an aerosol; or 311 (ii) for unprocessed cannabis flower, a container described in Section 4-41a-602 that: 312 (A) contains cannabis flowers in a quantity that varies by no more than 10% from the 313stated weight at the time of packaging; 314 (B) at any time the medical cannabis cardholder transports or possesses the container in 315public, is contained within an opaque bag or box that the medical cannabis pharmacy provides; 316and 317 (C) is labeled with the container's content and weight, the date of purchase, the legal 318use termination date, and after December 31, 2020, a barcode that provides information 319connected to an inventory control system; and 320 (iii) a form measured in grams, milligrams, or milliliters. 321 (b) "Medicinal dosage form" includes a portion of unprocessed cannabis flower that: 322 (i) the medical cannabis cardholder has recently removed from the container described 323in Subsection (38)(a)(ii) for use; and 324 (ii) does not exceed the quantity described in Subsection (38)(a)(ii). 325 (c) "Medicinal dosage form" does not include: 326 (i) any unprocessed cannabis flower outside of the container described in Subsection 327(38)(a)(ii), except as provided in Subsection (38)(b); 328 (ii) any unprocessed cannabis flower in a container described in Subsection (38)(a)(ii) 329after the legal use termination date; 330 (iii) a process of vaporizing and inhaling concentrated cannabis by placing the cannabis 331on a nail or other metal object that is heated by a flame, including a blowtorch; or 332 (iv) a liquid suspension that is branded as a beverage. 333 (39) "Nonresident patient" means an individual who: 334 (a) is not a resident of Utah or has been a resident of Utah for less than 45 days; 335 (b) has a currently valid medical cannabis card or the equivalent of a medical cannabis 336card under the laws of another state, district, territory, commonwealth, or insular possession of 337the United States; and H.B. 230 01-17-23 2:26 PM - 12 - 338 (c) has been diagnosed with a qualifying condition as described in Section 26-61a-104. 339 (40) "Payment provider" means an entity that contracts with a cannabis production 340establishment or medical cannabis pharmacy to facilitate transfers of funds between the 341establishment or pharmacy and other businesses or individuals. 342 (41) "Pharmacy medical provider" means the medical provider required to be on site at 343a medical cannabis pharmacy under Section 26-61a-403. 344 (42) "Provisional patient card" means a card that: 345 (a) the department issues to a minor with a qualifying condition for whom: 346 (i) a recommending medical provider has recommended a medical cannabis treatment; 347and 348 (ii) the department issues a medical cannabis guardian card to the minor's parent or 349legal guardian; and 350 (b) is connected to the electronic verification system. 351 (43) "Qualified medical provider" means an individual: 352 (a) who meets the recommending qualifications; and 353 (b) whom the department registers to recommend treatment with cannabis in a 354medicinal dosage form under Section 26-61a-106. 355 (44) "Qualified Patient Enterprise Fund" means the enterprise fund created in Section 35626-61a-109. 357 (45) "Qualifying condition" means a condition described in Section 26-61a-104. 358 (46) "Recommend" or "recommendation" means, for a recommending medical 359provider, the act of suggesting the use of medical cannabis treatment, which: 360 (a) certifies the patient's eligibility for a medical cannabis card; and 361 (b) may include, at the recommending medical provider's discretion, directions of use, 362with or without dosing guidelines. 363 (47) "Recommending medical provider" means a qualified medical provider or a 364limited medical provider. 365 (48) "Recommending qualifications" means that an individual: 366 (a) (i) has the authority to write a prescription; 367 (ii) is licensed to prescribe a controlled substance under Title 58, Chapter 37, Utah 368Controlled Substances Act; and 01-17-23 2:26 PM H.B. 230 - 13 - 369 (iii) possesses the authority, in accordance with the individual's scope of practice, to 370prescribe a Schedule II controlled substance; and 371 (b) is licensed as: 372 (i) a podiatrist under Title 58, Chapter 5a, Podiatric Physician Licensing Act; 373 (ii) an advanced practice registered nurse under Title 58, Chapter 31b, Nurse Practice 374Act; 375 (iii) a physician under Title 58, Chapter 67, Utah Medical Practice Act, or Title 58, 376Chapter 68, Utah Osteopathic Medical Practice Act; or 377 (iv) a physician assistant under Title 58, Chapter 70a, Utah Physician Assistant Act. 378 (49) "State central patient portal" means the website the department creates, in 379accordance with Section 26-61a-601, to facilitate patient safety, education, and an electronic 380medical cannabis order. 381 (50) "State central patient portal medical provider" means a physician or pharmacist 382that the department employs in relation to the state central patient portal to consult with 383medical cannabis cardholders in accordance with Section 26-61a-602. 384 (51) "State electronic verification system" means the system described in Section 38526-61a-103. 386 (52) "Tetrahydrocannabinol" or "THC" means a substance derived from cannabis or a 387synthetic equivalent as described in Subsection 58-37-4(2)(a)(iii)(AA). 388 (53) "THC analog" means the same as that term is defined in Section 4-41-102. 389 (54) "Valid form of photo identification" means any of the following forms of 390identification that is either current or has expired within the previous six months: 391 (a) a valid state-issued driver license or identification card; 392 (b) a valid United States federal-issued photo identification, including: 393 (i) a United States passport; 394 (ii) a United States passport card; 395 (iii) a United States military identification card; or 396 (iv) a permanent resident card or alien registration receipt card; or 397 (c) a passport that another country issued. 398 Section 3. Section 26-61a-105 is amended to read: 399 26-61a-105. Compassionate Use Board. H.B. 230 01-17-23 2:26 PM - 14 - 400 (1) (a) The department shall establish a Compassionate Use Board consisting of: 401 (i) seven qualified medical providers that the executive director appoints and the 402Senate confirms: 403 (A) who are knowledgeable about the medicinal use of cannabis; 404 (B) who are physicians licensed under Title 58, Chapter 67, Utah Medical Practice Act, 405or Title 58, Chapter 68, Utah Osteopathic Medical Practice Act; and 406 (C) whom the appropriate board certifies in the specialty of neurology, pain medicine 407and pain management, medical oncology, psychiatry, infectious disease, internal medicine, 408pediatrics, or gastroenterology; and 409 (ii) as a nonvoting member and the chair of the Compassionate Use Board, the 410executive director or the director's designee. 411 (b) In appointing the seven qualified medical providers described in Subsection (1)(a), 412the executive director shall ensure that at least two have a board certification in pediatrics. 413 (2) (a) Of the members of the Compassionate Use Board that the executive director 414first appoints: 415 (i) three shall serve an initial term of two years; and 416 (ii) the remaining members shall serve an initial term of four years. 417 (b) After an initial term described in Subsection (2)(a) expires: 418 (i) each term is four years; and 419 (ii) each board member is eligible for reappointment. 420 (c) A member of the Compassionate Use Board may serve until a successor is 421appointed. 422 (3) Four members constitute a quorum of the Compassionate Use Board. 423 (4) A member of the Compassionate Use Board may receive: 424 (a) notwithstanding Section 63A-3-106, compensation or benefits for the member's 425service; and 426 (b) travel expenses in accordance with Section 63A-3-107 and rules made by the 427Division of Finance in accordance with Section 63A-3-107. 428 (5) The Compassionate Use Board shall: 429 (a) review and recommend for department approval a petition to the board regarding an 430individual described in Subsection 26-61a-201(2)(a), a minor described in Subsection 01-17-23 2:26 PM H.B. 230 - 15 - 43126-61a-201(2)(c), or an individual who is not otherwise qualified to receive a medical cannabis 432card to obtain a medical cannabis card for compassionate use, for the standard or a reduced 433period of validity, if: 434 (i) for an individual who is not otherwise qualified to receive a medical cannabis card, 435the individual's qualified medical provider is actively treating the individual for an intractable 436condition that: 437 (A) substantially impairs the individual's quality of life; and 438 (B) has not, in the qualified medical provider's professional opinion, adequately 439responded to conventional treatments; 440 (ii) the qualified medical provider: 441 (A) recommends that the individual or minor be allowed to use medical cannabis; and 442 (B) provides a letter, relevant treatment history, and notes or copies of progress notes 443describing relevant treatment history including rationale for considering the use of medical 444cannabis; and 445 (iii) the Compassionate Use Board determines that: 446 (A) the recommendation of the individual's qualified medical provider is justified; and 447 (B) based on available information, it may be in the best interests of the individual to 448allow the use of medical cannabis; 449 (b) review and approve or deny the use of a medical cannabis device for an individual 450described in Subsection 26-61a-201(2)(a)(i)(B) or a minor described in Subsection 45126-61a-201(2)(c) if the individual's or minor's qualified medical provider recommends that the 452individual or minor be allowed to use a medical cannabis device to vaporize the medical 453cannabis treatment; 454 (c) unless no petitions are pending: 455 (i) meet to receive or review compassionate use petitions at least quarterly; and 456 (ii) if there are more petitions than the board can receive or review during the board's 457regular schedule, as often as necessary; 458 (d) except as provided in Subsection (6), complete a review of each petition and 459recommend to the department approval or denial of the applicant for qualification for a medical 460cannabis card within 90 days after the day on which the board received the petition; 461 (e) consult with the department regarding the criteria described in Subsection (6); and H.B. 230 01-17-23 2:26 PM - 16 - 462 (f) report, before November 1 of each year, to the Health and Human Services Interim 463Committee: 464 (i) the number of compassionate use recommendations the board issued during the past 465year; and 466 (ii) the types of conditions for which the board recommended compassionate use. 467 (6) The department shall make rules, in consultation with the Compassionate Use 468Board and in accordance with Title 63G, Chapter 3, Utah Administrative Rulemaking Act, to 469establish a process and criteria for a petition to the board to automatically qualify for expedited 470final review and approval or denial by the department in cases where, in the determination of 471the department and the board: 472 (a) time is of the essence; 473 (b) engaging the full review process would be unreasonable in light of the petitioner's 474physical condition; and 475 (c) sufficient factors are present regarding the petitioner's safety. 476 (7) (a) (i) The department shall review: 477 (A) any compassionate use for which the Compassionate Use Board recommends 478approval under Subsection (5)(d) to determine whether the board properly exercised the board's 479discretion under this section; and 480 (B) any expedited petitions the department receives under the process described in 481Subsection (6). 482 (ii) If the department determines that the Compassionate Use Board properly exercised 483the board's discretion in recommending approval under Subsection (5)(d) or that the expedited 484petition merits approval based on the criteria established in accordance with Subsection (6), the 485department shall: 486 (A) issue the relevant medical cannabis card; and 487 (B) provide for the renewal of the medical cannabis card in accordance with the 488recommendation of the qualified medical provider described in Subsection (5)(a). 489 (b) (i) If the Compassionate Use Board recommends denial under Subsection (5)(d), 490the individual seeking to obtain a medical cannabis card may petition the department to review 491the board's decision. 492 (ii) If the department determines that the Compassionate Use Board's recommendation 01-17-23 2:26 PM H.B. 230 - 17 - 493for denial under Subsection (5)(d) was arbitrary or capricious: 494 (A) the department shall notify the Compassionate Use Board of the department's 495determination; and 496 (B) the board shall reconsider the Compassionate Use Board's refusal to recommend 497approval under this section. 498 (c) In reviewing the Compassionate Use Board's recommendation for approval or 499denial under Subsection (5)(d) in accordance with this Subsection (7), the department shall 500presume the board properly exercised the board's discretion unless the department determines 501that the board's recommendation was arbitrary or capricious. 502 (8) Any individually identifiable health information contained in a petition that the 503Compassionate Use Board or department receives under this section is a protected record in 504accordance with Title 63G, Chapter 2, Government Records Access and Management Act. 505 [(9) The Compassionate Use Board shall annually report the board's activity to the 506Cannabis Research Review Board.] 507 Section 4. Section 26-61a-201 is amended to read: 508 26-61a-201. Medical cannabis patient card -- Medical cannabis guardian card -- 509Conditional medical cannabis card -- Application -- Fees -- Studies. 510 (1) (a) The department shall, within 15 days after the day on which an individual who 511satisfies the eligibility criteria in this section or Section 26-61a-202 submits an application in 512accordance with this section or Section 26-61a-202: 513 (i) issue a medical cannabis patient card to an individual described in Subsection 514(2)(a); 515 (ii) issue a medical cannabis guardian card to an individual described in Subsection 516(2)(b); 517 (iii) issue a provisional patient card to a minor described in Subsection (2)(c); and 518 (iv) issue a medical cannabis caregiver card to an individual described in Subsection 51926-61a-202(4). 520 (b) (i) Beginning on the earlier of September 1, 2021, or the date on which the 521electronic verification system is functionally capable of facilitating a conditional medical 522cannabis card under this Subsection (1)(b), upon the entry of a recommending medical 523provider's medical cannabis recommendation for a patient in the state electronic verification H.B. 230 01-17-23 2:26 PM - 18 - 524system, either by the provider or the provider's employee or by a medical cannabis pharmacy 525medical provider or medical cannabis pharmacy in accordance with Subsection 52626-61a-501(10)(a), the department shall issue to the patient an electronic conditional medical 527cannabis card, in accordance with this Subsection (1)(b). 528 (ii) A conditional medical cannabis card is valid for the lesser of: 529 (A) 60 days; or 530 (B) the day on which the department completes the department's review and issues a 531medical cannabis card under Subsection (1)(a), denies the patient's medical cannabis card 532application, or revokes the conditional medical cannabis card under Subsection (8). 533 (iii) The department may issue a conditional medical cannabis card to an individual 534applying for a medical cannabis patient card for which approval of the Compassionate Use 535Board is not required. 536 (iv) An individual described in Subsection (1)(b)(iii) has the rights, restrictions, and 537obligations under law applicable to a holder of the medical cannabis card for which the 538individual applies and for which the department issues the conditional medical cannabis card. 539 (2) (a) An individual is eligible for a medical cannabis patient card if: 540 (i) (A) the individual is at least 21 years old; or 541 (B) the individual is 18, 19, or 20 years old, the individual petitions the Compassionate 542Use Board under Section 26-61a-105, and the Compassionate Use Board recommends 543department approval of the petition; 544 (ii) the individual is a Utah resident; 545 (iii) the individual's recommending medical provider recommends treatment with 546medical cannabis in accordance with Subsection (4); 547 (iv) the individual signs an acknowledgment stating that the individual received the 548information described in Subsection (9); and 549 (v) the individual pays to the department a fee in an amount that, subject to Subsection 55026-61a-109(5), the department sets in accordance with Section 63J-1-504. 551 (b) (i) An individual is eligible for a medical cannabis guardian card if the individual: 552 (A) is at least 18 years old; 553 (B) is a Utah resident; 554 (C) is the parent or legal guardian of a minor for whom the minor's qualified medical 01-17-23 2:26 PM H.B. 230 - 19 - 555provider recommends a medical cannabis treatment, the individual petitions the Compassionate 556Use Board under Section 26-61a-105, and the Compassionate Use Board recommends 557department approval of the petition; 558 (D) the individual signs an acknowledgment stating that the individual received the 559information described in Subsection (9); 560 (E) pays to the department a fee in an amount that, subject to Subsection 56126-61a-109(5), the department sets in accordance with Section 63J-1-504, plus the cost of the 562criminal background check described in Section 26-61a-203; and 563 (F) the individual has not been convicted of a misdemeanor or felony drug distribution 564offense under either state or federal law, unless the individual completed any imposed sentence 565six months or more before the day on which the individual applies for a medical cannabis 566guardian card. 567 (ii) The department shall notify the Department of Public Safety of each individual that 568the department registers for a medical cannabis guardian card. 569 (c) (i) A minor is eligible for a provisional patient card if: 570 (A) the minor has a qualifying condition; 571 (B) the minor's qualified medical provider recommends a medical cannabis treatment 572to address the minor's qualifying condition; 573 (C) one of the minor's parents or legal guardians petitions the Compassionate Use 574Board under Section 26-61a-105, and the Compassionate Use Board recommends department 575approval of the petition; and 576 (D) the minor's parent or legal guardian is eligible for a medical cannabis guardian card 577under Subsection (2)(b) or designates a caregiver under Subsection (2)(d) who is eligible for a 578medical cannabis caregiver card under Section 26-61a-202. 579 (ii) The department shall automatically issue a provisional patient card to the minor 580described in Subsection (2)(c)(i) at the same time the department issues a medical cannabis 581guardian card to the minor's parent or legal guardian. 582 (d) Beginning on the earlier of September 1, 2021, or the date on which the electronic 583verification system is functionally capable of servicing the designation, if the parent or legal 584guardian of a minor described in Subsections (2)(c)(i)(A) through (C) does not qualify for a 585medical cannabis guardian card under Subsection (2)(b), the parent or legal guardian may H.B. 230 01-17-23 2:26 PM - 20 - 586designate up to two caregivers in accordance with Subsection 26-61a-202(1)(c) to ensure that 587the minor has adequate and safe access to the recommended medical cannabis treatment. 588 (3) (a) An individual who is eligible for a medical cannabis card described in 589Subsection (2)(a) or (b) shall submit an application for a medical cannabis card to the 590department: 591 (i) through an electronic application connected to the state electronic verification 592system; 593 (ii) with the recommending medical provider; and 594 (iii) with information including: 595 (A) the applicant's name, gender, age, and address; 596 (B) the number of the applicant's valid form of photo identification; 597 (C) for a medical cannabis guardian card, the name, gender, and age of the minor 598receiving a medical cannabis treatment under the cardholder's medical cannabis guardian card; 599and 600 (D) for a provisional patient card, the name of the minor's parent or legal guardian who 601holds the associated medical cannabis guardian card. 602 (b) The department shall ensure that a medical cannabis card the department issues 603under this section contains the information described in Subsection (3)(a)(iii). 604 (c) (i) If a recommending medical provider determines that, because of age, illness, or 605disability, a medical cannabis patient cardholder requires assistance in administering the 606medical cannabis treatment that the recommending medical provider recommends, the 607recommending medical provider may indicate the cardholder's need in the state electronic 608verification system, either directly or, for a limited medical provider, through the order 609described in Subsections 26-61a-106(1)(c) and (d). 610 (ii) If a recommending medical provider makes the indication described in Subsection 611(3)(c)(i): 612 (A) the department shall add a label to the relevant medical cannabis patient card 613indicating the cardholder's need for assistance; 614 (B) any adult who is 18 years old or older and who is physically present with the 615cardholder at the time the cardholder needs to use the recommended medical cannabis 616treatment may handle the medical cannabis treatment and any associated medical cannabis 01-17-23 2:26 PM H.B. 230 - 21 - 617device as needed to assist the cardholder in administering the recommended medical cannabis 618treatment; and 619 (C) an individual of any age who is physically present with the cardholder in the event 620of an emergency medical condition, as that term is defined in Section 31A-1-301, may handle 621the medical cannabis treatment and any associated medical cannabis device as needed to assist 622the cardholder in administering the recommended medical cannabis treatment. 623 (iii) A non-cardholding individual acting under Subsection (3)(c)(ii)(B) or (C) may not: 624 (A) ingest or inhale medical cannabis; 625 (B) possess, transport, or handle medical cannabis or a medical cannabis device outside 626of the immediate area where the cardholder is present or with an intent other than to provide 627assistance to the cardholder; or 628 (C) possess, transport, or handle medical cannabis or a medical cannabis device when 629the cardholder is not in the process of being dosed with medical cannabis. 630 (4) To recommend a medical cannabis treatment to a patient or to renew a 631recommendation, a recommending medical provider shall: 632 (a) before recommending or renewing a recommendation for medical cannabis in a 633medicinal dosage form or a cannabis product in a medicinal dosage form: 634 (i) verify the patient's and, for a minor patient, the minor patient's parent or legal 635guardian's valid form of identification described in Subsection (3)(a); 636 (ii) review any record related to the patient and, for a minor patient, the patient's parent 637or legal guardian in: 638 (A) for a qualified medical provider, the state electronic verification system; and 639 (B) the controlled substance database created in Section 58-37f-201; and 640 (iii) consider the recommendation in light of the patient's qualifying condition, history 641of substance use or opioid use disorder, and history of medical cannabis and controlled 642substance use during an initial face-to-face visit with the patient; and 643 (b) state in the recommending medical provider's recommendation that the patient: 644 (i) suffers from a qualifying condition, including the type of qualifying condition; and 645 (ii) may benefit from treatment with cannabis in a medicinal dosage form or a cannabis 646product in a medicinal dosage form. 647 (5) (a) Except as provided in Subsection (5)(b) or (c), a medical cannabis card that the H.B. 230 01-17-23 2:26 PM - 22 - 648department issues under this section is valid for the lesser of: 649 (i) an amount of time that the recommending medical provider determines; or 650 (ii) (A) six months for the first issuance, and, except as provided in Subsection 651(5)(a)(ii)(B), for a renewal; or 652 (B) for a renewal, one year if, after at least one year following the issuance of the 653original medical cannabis card, the recommending medical provider determines that the patient 654has been stabilized on the medical cannabis treatment and a one-year renewal period is 655justified. 656 (b) (i) A medical cannabis card that the department issues in relation to a terminal 657illness described in Section 26-61a-104 expires after one year. 658 (ii) The recommending medical provider may revoke a recommendation that the 659provider made in relation to a terminal illness described in Section 26-61a-104 if the medical 660cannabis cardholder no longer has the terminal illness. 661 (c) A medical cannabis card that the department issues in relation to acute pain as 662described in Section 26-61a-104 expires 30 days after the day on which the department first 663issues a conditional or full medical cannabis card. 664 (6) (a) A medical cannabis patient card or a medical cannabis guardian card is 665renewable if: 666 (i) at the time of renewal, the cardholder meets the requirements of Subsection (2)(a) or 667(b); or 668 (ii) the cardholder received the medical cannabis card through the recommendation of 669the Compassionate Use Board under Section 26-61a-105. 670 (b) The recommending medical provider who made the underlying recommendation 671for the card of a cardholder described in Subsection (6)(a) may renew the cardholder's card 672through phone or video conference with the cardholder, at the recommending medical 673provider's discretion. 674 (c) Before having access to a renewed card, a cardholder under Subsection (2)(a) or (b) 675shall pay to the department a renewal fee in an amount that: 676 (i) subject to Subsection 26-61a-109(5), the department sets in accordance with Section 67763J-1-504; and 678 (ii) may not exceed the cost of the relatively lower administrative burden of renewal in 01-17-23 2:26 PM H.B. 230 - 23 - 679comparison to the original application process. 680 (d) If a minor meets the requirements of Subsection (2)(c), the minor's provisional 681patient card renews automatically at the time the minor's parent or legal guardian renews the 682parent or legal guardian's associated medical cannabis guardian card. 683 (7) (a) A cardholder under this section shall carry the cardholder's valid medical 684cannabis card with the patient's name. 685 (b) (i) A medical cannabis patient cardholder or a provisional patient cardholder may 686purchase, in accordance with this chapter and the recommendation underlying the card, 687cannabis in a medicinal dosage form, a cannabis product in a medicinal dosage form, or a 688medical cannabis device. 689 (ii) A cardholder under this section may possess or transport, in accordance with this 690chapter and the recommendation underlying the card, cannabis in a medicinal dosage form, a 691cannabis product in a medicinal dosage form, or a medical cannabis device. 692 (iii) To address the qualifying condition underlying the medical cannabis treatment 693recommendation: 694 (A) a medical cannabis patient cardholder or a provisional patient cardholder may use 695cannabis in a medicinal dosage form, a medical cannabis product in a medicinal dosage form, 696or a medical cannabis device; and 697 (B) a medical cannabis guardian cardholder may assist the associated provisional 698patient cardholder with the use of cannabis in a medicinal dosage form, a medical cannabis 699product in a medicinal dosage form, or a medical cannabis device. 700 (8) The department may revoke a medical cannabis card that the department issues 701under this section if the cardholder: 702 (a) violates this chapter; or 703 (b) is convicted under state or federal law of, after March 17, 2021, a drug distribution 704offense. 705 (9) The department shall establish by rule, in accordance with Title 63G, Chapter 3, 706Utah Administrative Rulemaking Act, a process to provide information regarding the following 707to an individual receiving a medical cannabis card: 708 (a) risks associated with medical cannabis treatment; 709 (b) the fact that a condition's listing as a qualifying condition does not suggest that H.B. 230 01-17-23 2:26 PM - 24 - 710medical cannabis treatment is an effective treatment or cure for that condition, as described in 711Subsection 26-61a-104(1); and 712 (c) other relevant warnings and safety information that the department determines. 713 (10) The department may establish procedures by rule, in accordance with Title 63G, 714Chapter 3, Utah Administrative Rulemaking Act, to implement the application and issuance 715provisions of this section. 716 (11) (a) On or before September 1, 2021, the department shall establish by rule, in 717accordance with Title 63G, Chapter 3, Utah Administrative Rulemaking Act, a process to allow 718an individual from another state to register with the department in order to purchase medical 719cannabis or a medical cannabis device from a medical cannabis pharmacy while the individual 720is visiting the state. 721 (b) The department may only provide the registration process described in Subsection 722(11)(a): 723 (i) to a nonresident patient; and 724 (ii) for no more than two visitation periods per calendar year of up to 21 calendar days 725per visitation period. 726 (12) (a) A person may submit to the department a request to conduct a research study 727using medical cannabis cardholder data that the state electronic verification system contains. 728 (b) The department shall review a request described in Subsection (12)(a) to determine 729whether an institutional review board[, as that term is defined in Section 26-61-102,] could 730approve the research study. 731 (c) At the time an individual applies for a medical cannabis card, the department shall 732notify the individual: 733 (i) of how the individual's information will be used as a cardholder; 734 (ii) that by applying for a medical cannabis card, unless the individual withdraws 735consent under Subsection (12)(d), the individual consents to the use of the individual's 736information for external research; and 737 (iii) that the individual may withdraw consent for the use of the individual's 738information for external research at any time, including at the time of application. 739 (d) An applicant may, through the medical cannabis card application, and a medical 740cannabis cardholder may, through the state central patient portal, withdraw the applicant's or 01-17-23 2:26 PM H.B. 230 - 25 - 741cardholder's consent to participate in external research at any time. 742 (e) The department may release, for the purposes of a study described in this 743Subsection (12), information about a cardholder under this section who consents to participate 744under Subsection (12)(c). 745 (f) If an individual withdraws consent under Subsection (12)(d), the withdrawal of 746consent: 747 (i) applies to external research that is initiated after the withdrawal of consent; and 748 (ii) does not apply to research that was initiated before the withdrawal of consent. 749 (g) The department may establish standards for a medical research study's validity, by 750rule made in accordance with Title 63G, Chapter 3, Utah Administrative Rulemaking Act. 751 (13) The department shall record the issuance or revocation of a medical cannabis card 752under this section in the controlled substance database. 753 Section 5. Section 26-61a-703 is amended to read: 754 26-61a-703. Report. 755 (1) By the November interim meeting each year beginning in 2020, the department 756shall report to the Health and Human Services Interim Committee on: 757 (a) the number of applications and renewal applications filed for medical cannabis 758cards; 759 (b) the number of qualifying patients and designated caregivers; 760 (c) the nature of the debilitating medical conditions of the qualifying patients; 761 (d) the age and county of residence of cardholders; 762 (e) the number of medical cannabis cards revoked; 763 (f) the number of practitioners providing recommendations for qualifying patients; 764 (g) the number of license applications and renewal license applications received; 765 (h) the number of licenses the department has issued in each county; 766 (i) the number of licenses the department has revoked; 767 (j) the quantity of medical cannabis shipments that the state central patient portal 768facilitates; 769 (k) the number of overall purchases of medical cannabis and medical cannabis products 770from each medical cannabis pharmacy; 771 (l) the expenses incurred and revenues generated from the medical cannabis program; H.B. 230 01-17-23 2:26 PM - 26 - 772and 773 (m) an analysis of product availability in medical cannabis pharmacies. 774 (2) The report shall include information provided by the Center for Medical Cannabis 775Research described in Section 53B-17-1402. 776 [(2)] (3) The department may not include personally identifying information in the 777report described in this section. 778 [(3)] (4) During the 2022 legislative interim, the department shall report to the working 779group described in Section 36-12-8.2 as requested by the working group. 780 Section 6. Section 53B-17-1401 is enacted to read: 781 CHAPTER 17. UNIVERSITY OF UTAH 782 Part 14. Center for Medical Cannabis Research 783 53B-17-1401. Definitions. 784 As used in this part: 785 (1) "Academic research cannabis license" means the license described in Title 4, 786Chapter 41a, Part 9, Academic Medical Cannabis Research. 787 (2) "Cannabis" means the same as that term is defined in Section 26-61a-102. 788 (3) "Cannabis cultivation facility" means the same as that term is defined in Section 7894-41a-102. 790 (4) "Cannabis product" means the same as that term is defined in Section 26-61a-102. 791 (5) "Center" means the Center for the Medical Cannabis Research created in Section 79253B-17-1402. 793 (6) "Eligible institution" means an institution of higher education that: 794 (a) is located in Utah; and 795 (b) has or will obtain an academic research cannabis license. 796 (7) "Medical cannabis patient card" means the same as that term is defined in Section 79726-61a-102. 798 Section 7. Section 53B-17-1402 is enacted to read: 799 53B-17-1402. Center creation -- Duties. 800 (1) There is created the Center for Medical Cannabis Research within the University of 801Utah. 802 (2) The center: 01-17-23 2:26 PM H.B. 230 - 27 - 803 (a) shall seek state, federal, and private funds to award grants for medical cannabis 804research; 805 (b) shall facilitate and support funding for research related to the health effects, 806including the potential risks or side effects, of the use of cannabis products; 807 (c) shall facilitate and support funding for research related to the efficacy and potential 808health effects of various cannabis delivery methods, including vaporizing, ingesting, topical 809application, and combustion; 810 (d) shall support researchers in applying for and securing federal and private research 811grant funding for expanding medical cannabis research; 812 (e) shall review current and future cannabis research literature, clinical studies, and 813clinical trials; 814 (f) shall educate medical providers, lawmakers, and the public about medical cannabis 815research advances; 816 (g) shall, if requested, consult with researchers and eligible institutions seeking to 817conduct medical cannabis research regarding legal implications of the research under state and 818federal law; 819 (h) shall monitor, to the extent that appropriate and sufficient data are available, patient 820outcomes in any state with a medicinal cannabis program; 821 (i) may coordinate, share knowledge, and share best practices with a state: 822 (i) that has a medical cannabis program; and 823 (ii) is conducting cannabis research; 824 (j) may award or facilitate funding for grants to an eligible institution for medical 825cannabis research, including research regarding the growing of a medical-grade cannabis plant 826that is used for a cannabis product; 827 (k) shall support a licensed cannabis cultivation facility to provide medical-grade 828cannabis products for research; 829 (l) shall make any research conducted by the center publicly available; 830 (m) shall maintain a catalog of all published scientific reports based on projects funded 831or managed by the center; 832 (n) shall ensure that an individual who agrees to use a cannabis product as part of a 833research project conducted by the center or a grantee has: H.B. 230 01-17-23 2:26 PM - 28 - 834 (i) a valid medical cannabis patient card from the state; or 835 (ii) if included in the research project as a resident of another state, the equivalent of a 836medical cannabis patient card under the laws of another state, district, territory, 837commonwealth, or insular possession of the United States; 838 (o) shall obtain an academic research cannabis license; 839 (p) may apply for, or assist an eligible institution to apply for, a federal cannabis 840cultivation registration to locate a cannabis cultivation site in Utah; and 841 (q) for the report described in Section 26-61a-703, shall provide information to the 842Department of Health and Human Services describing: 843 (i) all research projects that are funded by a grant awarded by the center, including 844which institution received the grant; and 845 (ii) all research projects conducted by the center. 846 (3) The University of Utah shall provide staff for the center. 847 Section 8. Repealer. 848 This bill repeals: 849 Section 26-61-101, Title. 850 Section 26-61-102, Definitions. 851 Section 26-61-103, Institutional review board -- Approved study of cannabis, a 852cannabinoid product, or an expanded cannabinoid product. 853 Section 26-61-201, Cannabis Research Review Board. 854 Section 26-61-202, Duties.