Corrine Lucas is the Director of Regulatory Affairs for TerumoBCT Inc. and is responsible for identifying and implementing global regulatory initiatives and supporting global registrations focusing on the transition to the EU MDR.Prior to joining TerumoBCT, Corrine was an independent regulatory and quality systems consultant assisting medical device manufacturers with regulatory strategies and submissions as well as the implementation of compliant quality systems including auditing, training, and correcting deficiencies found during FDA, state, or notified body inspections across a broad range of product types including cardiovascular, ophthalmic, orthopedic, surgical, software, IVDs, and dental. Corrine also participated as a mentor for the Nordic Mentor Network for Entrepreneurship (NOME) assisting early-stage life science companies with entry into the US market.