Parenteral Drug Association | Pharmaceutical Regulatory News
PDA is the global provider of science, technology, and regulatory information serving the pharmaceutical & biopharmaceutical industries. Explore PDA's Education, Trainings, Events, …
PDA Week 2026 | PDA
Mar 4, 2011 · Explore the future of pharmaceutical science, technology, and regulation with industry leaders and innovators at PDA Week 2026, taking place in Denver, CO from 22-27 March.
Global Event Calendar | PDA
Explore PDA's Global Event Calendar for upcoming conferences, workshops, and networking opportunities in pharmaceutical science and technology.
Join/Renew Membership | PDA
PDA welcomes members at all stages in their careers, from students just learning the industry, to seasoned professionals with years of experience behind them. To accommodate all who work …
About PDA | PDA
The Parenteral Drug Association (PDA) is the leading global provider of science, technology, and regulatory information. PDA creates awareness and understanding of important issues facing …
PDA Training Courses | Continuing Education for Pharmaceutical ...
PDA's training courses offer practical information & implementable solutions related to essential industry topics. Learn more about our continuing education courses!
EU GMP Annex 1. Implementation of Contamination Control …
Aug 14, 2025 · Then we will provide details of the different approaches suggested by the ECA Foundation and Parenteral Drug Association (PDA), as well as the 5M-based approach and …
Aseptic Processing & Sterilization Resources | PDA
PDA has been a recognized leader in the area of aseptic processing and sterilization for more than 70 years and offers a wealth of educational and technical resources to promote product …
PDA Standards Development
PDA is an ANSI accredited standards developer for the production and regulation of products in the scientific community. Contact us to learn more!
PDA Regulatory Commenting
Dec 9, 2025 · Below are the comments submitted by PDA on behalf of its members to a variety of global regulatory and pharmacopeial bodies. The documents are available for review to all PDA …