PDA Regulatory Conference 2025

Achieving CGMP Excellence: Sustainable Compliance Across the Lifecycle
Returning to Washington, DC for the 34th year, PDA’s annual September regulatory conference remains the pharmaceutical industry’s most trusted forum for open, informed dialogue between global regulators and pharmaceutical professionals.

The PDA Regulatory Conference 2025 builds on this legacy with a robust agenda focused on advancing effective quality systems across the product lifecycle. Sessions will explore proven strategies for managing manufacturing and quality risks while driving operational excellence and sustainable compliance.

With strong U.S. FDA participation woven throughout the program, the Conference will spotlight critical CGMP pillars–including quality systems, facility and process design, supplier oversight, industrial modernization, and quality risk management. Real-world case studies–many shaped by regulator insights–will demonstrate how sustainable compliance translates into consistent product quality and a reliable supply chain.