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The session will give you an understanding on concepts of Process Validation lifecycle, the relationships between QbD, PPQ or CPV activities. The presentation will cover some recent regulatory trends and how to practically apply the theories during execution.


Process validation has been an integral part of the cGMPs. Proving documented evidence of process adequacy has been considered as an organizational milestone for years. The same set of justifications live through multiple inspection scrutiny during the products lifecycle. Hence it has always been, and continues to be, a mechanism to provide excessively convincing proof of the process being in a qualified state at all times. If we consider the 1987 process validation guidance as a first step, the 2011 guidance is indeed a new approach needing a different mindset. The recent regulatory inspection trend indicates continued difficulties in adhering with the latest 2011 regulations. Let’s understand the guidance purpose and consciously embrace them. New process validation practitioners should find it easier to adopt the 2011 guidance and excel in practice as they are not encumbered with the previous approaches.

Event Location

Online, Zoom, a link will be send prior the event.

Event Agenda

  • Genesis
  • Conceptual Differences: Current Vs Past PV
  • Enablers: Risk Assessment, Statistics
  • Stage 1- Process Design
  • Stage 2- Process Qualification
  • Stage 3- Continued Process Verification
  • Knowledge Management
  • Regulatory Actions
  • Legacy Products
  • References
  • Q&A

Attendee Registration

Registration closes on 27 July 2021 at 10AM.

Registration Category

ISPE Member