15.03.250 Packaging
(a) The registered entity shall package the final form of the approved medical marijuana product at the manufacturing site. The original seal shall not be broken except for quality testing at an approved laboratory, for adverse event investigations, by the Authority, by the certified patient or designated caregiver, or by the registered entity for internal quality control testing or disposal.
(b) The registered entity shall package the approved medical marijuana product such that it is child-resistant, tamper-proof/tamper-evident, light-resistant, and in a resealable package that minimizes oxygen exposure.
(c) The registered entity shall identify each lot of approved medical marijuana product with a lot unique identifier.