A manufacturing facility must have a certificate of authenticity or similar documentation approved by the department for all ingredients used in formulating a medical cannabinoid product. A certificate of authenticity or similar documentation approved by the department must include the date of expiration. Nonmarijuana ingredients for a medical cannabinoid product intended for ingestion must be of food-grade quality.

History: Effective July 1, 2022; amended effective October 1, 2025.

Law Implemented: NDCC 19-24.1-24.1, 19-24.1-36