Minnesota 2025-2026 Regular Session

Minnesota Senate Bill SF3349 Latest Draft

Bill / Introduced Version Filed 04/07/2025

                            1.1	A bill for an act​
1.2 relating to cannabis; requiring health care facilities to accommodate cannabis and​
1.3 hemp products; amending Minnesota Statutes 2024, section 342.56, subdivision​
1.4 2.​
1.5BE IT ENACTED BY THE LEGISLATURE OF THE STATE OF MINNESOTA:​
1.6 Section 1. Minnesota Statutes 2024, section 342.56, subdivision 2, is amended to read:​
1.7 Subd. 2.Health care facilities.(a) Health care facilities licensed under chapter 144A;​
1.8hospice providers licensed under chapter 144A; boarding care homes or supervised living​
1.9facilities licensed under section 144.50; assisted living facilities under chapter 144G; facilities​
1.10owned, controlled, managed, or under common control with hospitals licensed under chapter​
1.11144; and other health care facilities licensed by the commissioner of health or the​
1.12commissioner of human services may adopt reasonable restrictions on the use of medical​
1.13cannabis flower or medical, cannabinoid products, lower-potency hemp edibles, hemp-derived​
1.14consumer products, or hemp-derived topical products by a patient enrolled in the registry​
1.15program who resides at or is actively receiving treatment or care at the facility. The​
1.16restrictions may include a provision that the facility must not store or maintain a patient's​
1.17supply of medical cannabis flower or medical cannabinoid products on behalf of the patient;​
1.18that a patient store the patient's supply of medical cannabis flower or medicinal, cannabinoid​
1.19products, lower-potency hemp edibles, hemp-derived consumer products, or hemp-derived​
1.20topical products in a locked container accessible only to the patient, the patient's designated​
1.21caregiver, or the patient's parent, legal guardian, or spouse; that the facility is not responsible​
1.22for providing medical cannabis or hemp for patients; and that medical cannabis flower or​
1.23medical, cannabinoid products, lower-potency hemp edibles, hemp-derived consumer​
1.24products, or hemp-derived topical products are used only in a location specified by the​
1​Section 1.​
25-04960 as introduced​03/20/25 REVISOR SS/LJ​
SENATE​
STATE OF MINNESOTA​
S.F. No. 3349​NINETY-FOURTH SESSION​
(SENATE AUTHORS: CLARK)​
OFFICIAL STATUS​D-PG​DATE​
Introduction and first reading​04/09/2025​
Referred to Commerce and Consumer Protection​ 2.1facility or provider. Nothing in this subdivision requires facilities and providers listed in​
2.2this subdivision to adopt such restrictions.​
2.3 (b) No facility or provider listed in this subdivision may unreasonably limit a patient's​
2.4access to or use of medical cannabis flower or medical cannabinoid products, lower-potency​
2.5hemp edibles, hemp-derived consumer products, or hemp-derived topical products to the​
2.6extent that such use is authorized under sections 342.51 to 342.59, or the patient is a visiting​
2.7patient authorized to use medical cannabis under the laws of their state of residence. No​
2.8facility or provider listed in this subdivision may prohibit a patient access to or use of medical​
2.9cannabis flower or medical cannabinoid products due solely to the fact that cannabis is a​
2.10controlled substance pursuant to the federal Uniform Controlled Substances Act. If a federal​
2.11regulatory agency, the United States Department of Justice, or the federal Centers for​
2.12Medicare and Medicaid Services takes one of the following actions, a facility or provider​
2.13may suspend compliance with this paragraph until the regulatory agency, the United States​
2.14Department of Justice, or the federal Centers for Medicare and Medicaid Services notifies​
2.15the facility or provider that it may resume permitting the use of medical cannabis flower or​
2.16medical, cannabinoid products, lower-potency hemp edibles, hemp-derived consumer​
2.17products, or hemp-derived topical products within the facility or in the provider's service​
2.18setting:​
2.19 (1) a federal regulatory agency or the United States Department of Justice initiates​
2.20enforcement action against a facility or provider related to the facility's compliance with​
2.21the medical cannabis program; or​
2.22 (2) a federal regulatory agency, the United States Department of Justice, or the federal​
2.23Centers for Medicare and Medicaid Services issues a rule or otherwise provides notification​
2.24to the facility or provider that expressly prohibits the use of medical cannabis in health care​
2.25facilities or otherwise prohibits compliance with the medical cannabis program.​
2.26 (c) An employee or agent of a facility or provider listed in this subdivision or a person​
2.27licensed under chapter 144E is not violating this chapter or chapter 152 for the possession​
2.28of medical cannabis flower or medical cannabinoid products while carrying out employment​
2.29duties, including providing or supervising care to a patient enrolled in the registry program,​
2.30or distribution of medical cannabis flower or medical cannabinoid products to a patient​
2.31enrolled in the registry program who resides at or is actively receiving treatment or care at​
2.32the facility or from the provider with which the employee or agent is affiliated.​
2.33 (d) Nothing in this subdivision is intended to require a facility covered by this subdivision​
2.34to permit violations of sections 144.411 to 144.417.​
2​Section 1.​
25-04960 as introduced​03/20/25 REVISOR SS/LJ​