In a long-awaited decision released this morning, the United States Drug Enforcement Administration announced that it has denied two petitions to reschedule marijuana under the Controlled Substances Act (the “CSA”). The DEA concluded that marijuana should remain a Schedule I controlled substance because it does not meet the criteria for currently accepted medical use in treatment in the United States; there is a lack of accepted safety for use of marijuana under medical supervision and it has a high potential for abuse. The DEA’s decision relies on a scientific and medical evaluation and scheduling recommendation from the United States Department of Health and Human Services (“HHS”), based on studies conducted by the United States Food and Drug Administration and National Institute on Drug Abuse (“NIDA”).
The DEA’s decision represents a blow to proponents of federal legalization of marijuana for medical and recreational use, and marks the continuation of the uncomfortable status quo of conflicting state and federal classification of marijuana that marijuana businesses and consumers face in states that have legalized the production, sale and consumption of marijuana. Accordingly, access to banking and other financial services, the threat of federal prosecution and the application of Internal Revenue Code Section 280E to marijuana businesses will continue to be issues faced in this emerging industry.
The DEA also announced a policy change that opens the door to expanded marijuana research efforts by increasing the number of DEA-registered marijuana manufacturers. Currently, only the University of Mississippi, acting through a contract with NIDA, holds DEA authorization to supply marijuana to researchers, who must also be registered with the DEA, in the United States. This has led some of the 350 currently registered marijuana researchers to complain about a shortfall of supply and lack in the variety of marijuana strains available to them.
Under the new policy, the DEA will register marijuana growers outside of the NIDA-contract system to supply researchers with marijuana if the growers agree that marijuana will be distributed only with the DEA’s prior written approval. Additionally, growers will be authorized to supply only DEA-registered researchers whose research protocols have been determined by HHS to be scientifically meritorious. Notably, these limitations would appear to exclude licensed growers in states such as Washington who currently produce marijuana for recreational and medical markets from obtaining DEA authorization.
The DEA’s policy also appears to highlight uncertainty regarding DEA authorization and state laws regulating the production and sale of marijuana. For example, in Washington, an individual or business is allowed to grow marijuana only if it holds a license issued by the Washington State Liquor and Cannabis Board, and one of the conditions of the license is that state-licensed producers are allowed to sell marijuana only to other state-licensed producers or processors. Accordingly, any individual or business seeking DEA registration to produce and supply marijuana for research purposes will need to pay careful attention to applicable state laws when structuring their business.