QA020: SOP FOR PREPARATION, REVIEW, AND CONTROL OF VALIDATION MASTER PLAN (VMP)
OBJECTIVE: The purpose of this SOP is to define the procedure for the preparation, review, approval, issuance, and control of the Validation Master Plan (VMP) in compliance with WHO TRS / EU-GMP Annex 15 and other applicable regulatory guidelines. The VMP serves as a high-level document summarizing the site’s validation policy, strategy, responsibilities, scope, and […]