The Regulatory and Quality Compliance team at Bristol-Myers Squibb is responsible for ensuring that all biopharmaceutical products meet stringent regulatory standards and quality guidelines throughout their lifecycle. This includes overseeing regulatory submissions, ensuring compliance with Good Manufacturing Practices (GMP), conducting quality audits, and implementing pharmacovigilance strategies. The team's collaborative efforts help to safeguard patient safety while facilitating the timely delivery of innovative therapies to market.
View all