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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. Flora Pharma expects to fast track traditional FDA and NHS timelines by running phase trials in parallel (in vitro, in vivo, pilot in human, safety/efficacy, etc.).

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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 Organization Granted $12.9 Million to Study Cannabis and PTSD •

SpeedWeed

MAPS, The Multidisciplinary Association for Psychedelic Substances, was awarded a $12,979,050 million grant from the state of Michigan to fund a study on PTSD and cannabis on August 10. This grant enables more rigorous study, overseen by the FDA, which may lead to cannabis flower becoming prescribable medicine someday.

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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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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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Do you trust your doctor about cannabis?

The Cannigma

Barely a quarter of cannabis users trust their doctor to provide them with reliable information about medical cannabis and how to use it to treat their medical or health conditions, according to a recent survey. People want to trust their doctors, but doctors need knowledge. We have a ways to go,” Tan said.

Education 101