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MMJ International advances FDA-regulated cannabis medicine after marijuana’s reclassification to Schedule III, enabling clinical trials for Huntington’s and MS treatments.
MMJ International Holdings is advancing FDA-regulated cannabis medicine following the U.S. reclassification of marijuana from Schedule I to Schedule III, enabling formal pharmaceutical research.
The company, which has maintained FDA and DEA compliance for years, holds two active IND applications and FDA Orphan Drug Designations for treatments targeting Huntington’s disease and multiple sclerosis.
With a GMP-certified lab, precision dosing technology, and exclusive international partnerships, MMJ is positioned to lead U.S. clinical trials and European commercialization, emphasizing scientific rigor over political trends.
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MMJ International avanza en la medicina de cannabis regulada por la FDA después de la reclasificación de la marihuana en la Lista III, lo que permite ensayos clínicos para el tratamiento de la enfermedad de Huntington y la esclerosis múltiple.