Ruchira Kannambille

Ruchira is a Global Regulatory Affairs pharmaceutical professional with over 18 years of experience in CMC, Labeling, Promotional Review, Operations & Strategy across various therapeutic areas. In her role at Braeburn, Ruchira is responsible for leading all Regulatory Affairs activities while ensuring compliance with regulations and company policies. She has proven scientific, regulatory, and managerial expertise in full development programs, overseeing the preparation of and successful submissions of NDAs, INDs and ANDAs. Throughout her years, she has been able to lead and manage teams through complex regulatory submissions and interactions with numerous global health authorities, including the FDA, EMA, Health Canada and regional country authorities. Prior to joining Braeburn, Ruchira held various roles in increasing responsibilities in both brand and generic pharmaceutical companies. Ruchira earned her Bachelor of Science degree in Biomedical Engineering from Rutgers University.