6400.1 The provisions of this chapter shall apply to an individual or entity that is registered by the Board, or applying for a registration, to test medical cannabis and medical cannabis products.

6400.2 The provisions of this chapter do not apply to the in-house testing by a cultivation center of its own cultivated crop or products. However, a cultivation center shall not sell any of its cultivated crop or products until the crop or products have been tested and certified by an independent testing laboratory registered by the Board to test medical cannabis and medical cannabis products.

SOURCE: Final Rulemaking published at 66 DCR 10217 (August 9, 2019); as amended by Final Rulemaking published at 71 DCR 002388 (March 8, 2024); as amended by Final Rulemaking published at 73 DCR 002136 (February 20, 2026).