Registration for the 51st Annual GMP Conference opens December 1st, 2026!
About the Conference
The International GMP Conference and Medical Device Regulations (MDR) track were established to foster ongoing dialogue and collaboration among regulatory agencies, the pharmaceutical and medical device industries, and regulatory science professionals on critical compliance, quality, and innovation issues. These programs provide educational and networking opportunities that help shape the future of pharmaceutical, biologic, veterinary, and medical device advancement from a regulatory science perspective. Experienced leaders from the FDA, other major international regulatory agencies, industry, and consulting firms present and engage attendees on current and emerging issues, addressing both the strategic and practical implications of pharmaceutical manufacturing, quality systems, regulatory compliance, and FDA medical device regulations.