Required.
All cannabis and cannabis products must undergo laboratory testing by a licensed, accredited facility before retail sale. Each batch must be tested for cannabinoid potency and contaminants, and a Certificate of Analysis (COA)must be issued and retained in the state’s inventory tracking system. Manufacturers must reject and destroy any batch that fails to meet required testing thresholds.
Required.
Cannabinoid testing is mandatory for all product types. Required cannabinoids include (but may vary by product type):
Required if applicable.
Mandatory and defined by the Office of Cannabis Management.
All products must be tested for:
Testing panels vary slightly by product type (flower, concentrates, ingestible, topicals), and specific action limits are defined in rule appendices.
Most major contaminants are now regulated. However, product-specific exemptions or flexibilities in batch sizes/testing methods may result in occasional inconsistencies in enforcement.
Foreign material (e.g., hair, insects, plastic) is not yet a distinct testing category. .
Moderate Concern: Minnesota’s updated framework is robust but still implementing infrastructure for universal oversight. Lab licensing and enforcement systems are in early-stage rollout as of mid-2025.
Required
Minnesota Office of Cannabis Management
Website: https://mn.gov/cannabis
Phone: (651) 201-5598
Address: P.O. Box 64882, St. Paul, MN 55164
Email: cannabis.info@state.mn.us
Minnesota Health Department. (February 20, 2015) 4770.0500 Medical Cannabis Manufacturer; Quality Control; Assurance Program.
Minnesota Department of Health. (2020). Rule 4770.0500: Medical Cannabis Manufacturer Quality Control
Minnesota Office of Cannabis Management. (2025). Adult-Use Market Rules.
Cannabis Cate
We use cookies to analyze website traffic and optimize your website experience. By accepting our use of cookies, your data will be aggregated with all other user data.