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Flora Growth Forms Flora Pharma Division, Launches Global Clinical Trials

Cannabis Law Report

Flora Pharma will seek to identify scientific gaps in the cannabis industry and ultimately work to translate that to pharmaceutical cannabis products backed by data. The immediate next steps are to submit data for ethics committee review and approval whereupon acceptance, further details will be provided. “A

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MyMD Pharmaceuticals Announces New Data from Comparative Study on Lead Compound MYMD-1

Cannabis Law Report

New data shows MYMD-1 has key differentiators and capabilities compared to existing TNF inhibitor drugs. Company plans to initiate Phase II trial with a leading academic institution. These advanced analytics provide a human-centric, data-driven approach to phenotypic discovery for clients.”. Eurofins is testing for life.

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MAPS: Regulatory Publishing Specialist – Remote Position Regulatory Affairs · Any City, Any State, California

Cannabis Law Report

MAPS PBC strives to continually improve upon the supportive, equitable and accessible work environment. The RPS must enjoy working within a small, entrepreneurial environment in which the ability to work under pressure and to handle a wide variety of activities is necessary. Experience working for a clinical study Sponsor.

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MAPS Organization Granted $12.9 Million to Study Cannabis and PTSD •

SpeedWeed

This will be the second clinical trial to give cannabis medicine or placebos to participating military veterans, and according to the Chief Science Officer of the MAPS Public Benefit Corporation, Berra Yazar-Klosinki, PhD, the first trial was a great success. “We MAPS Makes History. The study was funded with $2.2

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Global Regulatory Specialist – Melbourne – Medicinal Cannabis i-Pharm Consulting Australia Pty Ltd

Cannabis Law Report

Support new product development and further clinical activities. Review clinical protocols to ensure the collection of data needed for regulatory submissions. Experience with prescription drug registration submissions and lifecycle management, including clinical trial activities. SKILLS/QUALIFICATIONS.

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Australia: Global Regulatory Specialist – Melbourne – Medicinal Cannabis i-Pharm Consulting Melbourne VIC

Cannabis Law Report

Support new product development and further clinical activities. Review clinical protocols to ensure the collection of data needed for regulatory submissions. Experience with prescription drug registration submissions and lifecycle management, including clinical trial activities. SKILLS/QUALIFICATIONS.

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Press Release: Canada – Princeton mushroom research and development facility officially opens, sells first grow of psilocybin mushrooms

Cannabis Law Report

And there are literally hundreds of trials that are being done, and more forthcoming.”. Ciprick said there needs to be more outcome data and studies on the psilocybin-producing mushrooms to give that comfort level heading forward into introducing a larger market for the product. I’m excited that we pulled our first crop down.