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Chris Robinson is a highly experienced regulatory professional with a solid background in the pharmaceutical and medical device industries. Currently serving as a Senior Regulatory Writer at Accorto Regulatory Solutions since April 2022, Chris manages various activities related to CMC sections for regulatory submissions, including authoring and reviewing documents. Previously, Chris held the position of Director of Research Development at Exela Pharma Sciences, leading a team to support CMC sections of ANDA/NDA filings for sterile injectable drug products. Additional experience includes positions as Associate Director of R&D at Ei Solutionworks and Manager of Launch Analytics and Sr. Manager of R&D at Boehringer Ingelheim, overseeing teams and enhancing laboratory efficiency. Chris holds both a Master’s and Bachelor’s degree in Chemistry from the University of North Carolina at Wilmington.