Risk Management in Sterile Manufacturing – Part 1

This 60-minute webcast will examine:

  • Best practices for risk management in sterile manufacturing
  • The application of quality-by design (QbD) principles in sterile manufacturing
  • FDA process validation guidelines


Patricia Van Arnum
Executive Editor
Pharmaceutical Technology and Pharmaceutical Technology Europe


Michael Curry
Director of Operations
DPT Lakewood, Center of Excellence for Aseptic and Specialty Products

Hal Baseman
Chief Operating Officer and Principal at ValSource LLC
Chair-Elect of the Parenteral Drug Association (PDA) Board of Directors, Vice-Chair of the PDA Science Advisory Board, and Co-Leader of the PDA Process Validation Interest Group

Dr. Mike Long, MBB
Director and Senior Consultant with ConcordiaValSource LLC
Co-chair of the Parenteral Drug Association’s (PDA) Risk Management Task Force and member of PDA’s Science Advisory Board

- Download Webinar (MP4, 60 MB)