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Andrew Charrette has over a decade of experience in regulatory affairs, project management, and medical writing, with a focus on the natural health product industry and clinical trials. Currently serving as the Director of Regulatory Affairs and Psychedelic Advisor at KGK Science Inc. since July 2013, Andrew has held several key positions including Senior Manager of Regulatory Affairs and Operations Director, ensuring the efficient management of clinical trial applications and quality assurance processes. Prior experience includes a role as a Medical Writer at Mediprobe Research Inc. and an Information Analyst at Brogan Inc. Andrew holds a Master of Science in Neuroscience from the University of Ottawa and a Bachelor of Medical Science in Pharmacology and Physiology from Western University.