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

Moderator:

Patricia Van Arnum
Executive Editor
Pharmaceutical Technology and Pharmaceutical Technology Europe

Speakers:

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)