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Christophe Tetar is a Senior Regulatory Affairs Consultant at EFOR, currently focusing on ensuring compliance with regulatory standards for the company's products. Previously, they served as a Regulatory Affairs Specialist at Cousin Biotech from 2008 to 2014, where they managed various pre-market approval files and registrations across multiple international markets. Since 2014, Christophe has been a Senior Regulatory Affairs Specialist at MacoPharma, handling complex regulatory documentation and approvals in line with stringent healthcare regulations. Christophe continues their education with a Mastère spécialisé in Normalisation, Qualité, Certification et Essais from UTC Compiégne and a Master 2 in Conception du médicament from Institut chimie pharmaceutique Albert Lespagnol Lille.