DEA Set to Launch Medical Marijuana Registration Forms for Manufacturers, Labs and Distributors

The Drug Enforcement Administration (DEA) is preparing to expand its medical marijuana registration system to cover more of the state-licensed supply chain, with new applications expected soon for manufacturers, growers, distributors and testing labs.

The move follows DEA’s recent launch of a registration portal and form for medical marijuana dispensaries, giving retailers a pathway to register for federal protections tied to the Trump administration’s ongoing marijuana rescheduling process. That initial form, however, applied only to dispensaries, leaving cultivators, processors, labs and distributors without a clear option during the 60-day expedited registration window.

DEA now says the registration pathway will be extended to other businesses involved in bringing state-licensed medical marijuana products from cultivation to testing and distribution. The forms are expected to be posted through the agency’s Diversion Control Division, though DEA has not announced a specific release date.

The new registration system is tied to DOJ’s recent rescheduling order, which places state-regulated medical marijuana products and FDA-approved marijuana products in Schedule III rather than Schedule I. A June 29 hearing is set for the full rescheduling of cannabis.

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