Process Challenge Device Development for EO Sterilization 2019
26 Mar 2019
Webinar
Description
Topics
What makes an appropriate PCD?
What is the purpose of the PCD?
How can you ensure consistency in your PCDs?
Are the requirements for PCDs different during validation versus routine processing?
When is requalification of PCDs required?
How should you evaluate or compare PCDs?
Who should Attend
Attendees from companies that produce sterile products, including:
Validation specialists
QA personnel
R&D specialists
Manufacturing personnel involved in sterilization
Past Events
Process Challenge Device Development for EO Sterilization 2019 - 26 Mar 2019, Webinar (50779)
Important
Please, check "Process Challenge Device Development for EO Sterilization" official website for possible changes, before making any traveling arrangements
