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The FDA-approved MMJ BioPharma awaits federal approval for 2,500 days despite meeting all legal requirements, violating a 60-day review mandate.
The DOJ’s September admission that the DEA’s internal courts are unconstitutional has spotlighted the stalled federal license application of MMJ BioPharma, which has waited over 2,500 days for approval despite meeting all legal and regulatory requirements, including FDA orphan drug designations and a Schedule I research license.
The delay violates the 60-day review mandate of the 2022 Medical Marijuana and Cannabidiol Research Expansion Act, hindering critical research into cannabinoid treatments for Huntington’s disease and multiple sclerosis.
With a failed phase 2 trial for SAGE-718 increasing urgency, experts urge President Trump to act—by approving MMJ’s license, creating a DEA medical research division, and ensuring DOJ oversight—to align federal policy with science and the rule of law.
El MMJ BioPharma aprobado por la FDA espera la aprobación federal durante 2.500 días a pesar de cumplir con todos los requisitos legales, violando un mandato de revisión de 60 días.