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
4 mrt. 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 …
14 aug. 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
9 dec. 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 …