-
Starmer faces MPs as pressure grows over Mandelson scandal
-
HRW urges pushback against 'aggressive superpowers'
-
Russia demands Ukraine give in as UAE talks open
-
Gaza civil defence says 17 killed in strikes after Israel says shots wounded officer
-
France's Kante joins Fenerbahce after Erdogan 'support'
-
CK Hutchison launches arbitration over Panama Canal port ruling
-
Stocks mostly rise as traders ignore AI-fuelled sell-off on Wall St
-
Acclaimed Iraqi film explores Saddam Hussein's absurd birthday rituals
-
On rare earth supply, Trump for once seeks allies
-
Ukrainian chasing sumo greatness after meteoric rise
-
Draper to make long-awaited return in Davis Cup qualifier
-
Can Ilia Malinin fulfil his promise at the Winter Olympics?
-
CK Hutchison begins arbitration against Panama over annulled canal contract
-
UNESCO recognition inspires hope in Afghan artist's city
-
Ukraine, Russia, US negotiators gather in Abu Dhabi for war talks
-
WTO must 'reform or die': talks facilitator
-
Doctors hope UK archive can solve under-50s bowel cancer mystery
-
Stocks swing following latest AI-fuelled sell-off on Wall St
-
Demanding Dupont set to fire France in Ireland opener
-
Britain's ex-prince Andrew leaves Windsor home: BBC
-
Coach plots first South Africa World Cup win after Test triumph
-
Spin-heavy Pakistan hit form, but India boycott risks early T20 exit
-
Japan eyes Premier League parity by aligning calendar with Europe
-
Whack-a-mole: US academic fights to purge his AI deepfakes
-
Love in a time of war for journalist and activist in new documentary
-
'Unprecedented mass killing': NGOs battle to quantify Iran crackdown scale
-
Seahawks kid Cooper Kupp seeks new Super Bowl memories
-
Thousands of Venezuelans march to demand Maduro's release
-
AI, manipulated images falsely link some US politicians with Epstein
-
Move on, says Trump as Epstein files trigger probe into British politician
-
Seven Oshyn Experts Honored with 2026 Sitecore Most Valuable Professional Awards
-
Vanderbilt Report: Coeptis Therapeutics Shareholders Approve Transformational Merger: From Biopharma to Dual-Sector Platform
-
Vanderbilt Report: NextTrip's 'Watch It, Book It' Model Gains Momentum as Revenue Surges and Company Acquires 200M-Viewer Travel Platform
-
Vanderbilt Report: Global Clean Energy's AI Division Targets $54 Billion Market Opportunity
-
Transglobal Management Group Achieves Profitability Through Golf Industry Consolidation
-
Vanderbilt Report: RenX Enterprises Builds Technology-Driven Waste-to-Value Platform Through Strategic Asset Monetization and Premium Market Expansion
-
Vanderbilt Report Issues Coverage on Full Alliance Group Inc.
-
The Vanderbilt Report: Argo Graphene Solutions Advances from Concrete Validation to Cold-Climate Asphalt Testing
-
Vanderbilt Report: VisionWave's Strategic Acquisitions Position Company for Defense Market Expansion
-
Pantheon Resources PLC Announces Notice of AGM
-
Arteta backs Arsenal to build on 'magical' place in League Cup final
-
Evil Empire to underdogs: Patriots eye 7th Super Bowl
-
UBS grilled on Capitol Hill over Nazi-era probe
-
Guardiola 'hurt' by suffering caused in global conflicts
-
Marseille do their work early to beat Rennes in French Cup
-
Colombia's Petro, Trump hail talks after bitter rift
-
Trump signs spending bill ending US government shutdown
-
Arsenal sink Chelsea to reach League Cup final
-
Leverkusen sink St Pauli to book spot in German Cup semis
-
'We just need something positive' - Monks' peace walk across US draws large crowds
Trump Marijuana Schedule I to Science: How MMJ International Holdings Is Defining the New Era of FDA Cannabis Medicine
WASHINGTON, D.C., AL / ACCESS Newswire / October 5, 2025 / As the United States moves closer to officially rescheduling marijuana under the Controlled Substances Act, one company has already spent nearly a decade building what the new regulatory era demands: pharmaceutical-grade cannabis medicines developed under FDA supervision.

MMJ International Holdings, through its subsidiaries MMJ BioPharma Cultivation and MMJ BioPharma Labs, is pioneering a scientific pathway that separates medicine from marijuana The company's research targets two debilitating neurological conditions - Huntington's disease and Multiple Sclerosis - one of which have earned FDA Orphan Drug Designations for MMJ's proprietary cannabinoid soft gel formulations (MMJ-001 and MMJ-002).
A Turning Point for Cannabis Science
After more than fifty years under Schedule I classification, marijuana's reclassification to Schedule III represents more than just a policy shift - it's an invitation to science. For the first time, researchers and pharmaceutical developers can pursue cannabinoid therapies without the crushing weight of Schedule I restrictions that historically paralyzed innovation and investment.
Under Schedule III:
FDA-approved research can move forward with streamlined DEA registration.
Pharmaceutical manufacturing and clinical supply chains become legally sustainable.
Insurance and reimbursement pathways for cannabinoid-based medicines can finally emerge.
Pharmaceutical Partnerships, Global Distribution
MMJ has established exclusive agreements with International producers of pharmaceutical grade cannabis, and Pharmaceuticals, which distributes to several pharmacies across Europe.
These partnerships ensure that MMJ's cannabinoid formulations meet the stringent Good Manufacturing Practice (GMP) and Good Distribution Practice (GDP) standards required for human clinical trials - and ultimately, for prescription medicines.
By leveraging this transatlantic supply chain, MMJ is positioned to lead both U.S. clinical development and European commercialization as the regulatory barriers fall.
FDA Compliance: The Real Differentiator
Unlike companies chasing rescheduling headlines, MMJ has already done the hard work:
Two active IND filings with the FDA.
GMP-certified laboratory infrastructure through MMJ BioPharma Labs.
Pending DEA bulk manufacturing registration (Control No. W18134021E).
Validated pharmaceutical encapsulation technology for precision dosing.
This pharmaceutical approach transforms cannabis from a political issue into a medical innovation platform - one grounded in evidence, ethics, and patient need.
A New Era of Accountability and Access
The U.S. is entering a critical inflection point. Schedule III rescheduling will not only unlock research but also expose which companies truly meet FDA and DEA standards - and which have simply marketed around them.
"Real patients deserve real medicine," Boise added. "MMJ was founded to prove that cannabinoid science, when done properly, can stand alongside any other pharmaceutical therapy. We're not selling marijuana - we're delivering medicine."
About MMJ International Holdings
MMJ International Holdings is a pioneering biopharmaceutical company developing cannabis derived medicinesthrough FDA approved clinical trials. Its subsidiaries - MMJ BioPharma Cultivation and MMJ BioPharma Labs - operate within DEA and FDA regulatory frameworks to produce standardized, pharmaceutical grade cannabinoid formulations for the treatment of Huntington's disease and Multiple Sclerosis.
MMJ is represented by attorney Megan Sheehan.
CONTACT:
Madison Hisey
[email protected]
203-231-8583
SOURCE: MMJ International Holdings
View the original press release on ACCESS Newswire
M.King--AT