Validation Master Plan (VMP)

#pharmaceutical #csv #csa #validation #quality #qrm #riskmanagement #fda #compliance #gmp #ich
This session will make you understand the "Validation Master Plan (VMP)" requirements in line with the various guideline expectations for example - EUGMP annex 11, 21 CFR Part 11, GAMP5, PIC/S guide etc.
The agenda for this session is as below;
Importance of topic
Know your Trainer
Guideline Requirements – EU,FDA, GAMP
Validation Master Plan Preparation
Key elements of VMP
Common non-conformities with the VMP
Q&A
Vote of Thanks and contact details

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