Unwritten Requirements Master Validation Plan Training Course: Using DQ, IQ, OQ, PQ Protocols in Risk

DUBLIN--(BUSINESS WIRE)--Oct 28, 2025--

The "Master Validation Plan - The Unwritten Requirements Course (November 18, 2025)" training has been added to ResearchAndMarkets.com 's offering.

FDA Warning Letters and recent high-profile recalls indicate major cGMP deficiencies in many companies. One major failing is lack of sufficient or targeted risk-based company-wide V&V planning. Starting with a Master Validation Plan, evaluating its elements against ISO 14971 hazard analysis / risk management, allows development of meaningful product validations. The roles of different V&V protocols.

How to employ equipment / process DQs, IQs, OQs, and PQs, or their equivalents per ASTM E2500, against a background of limited company resources (personnel, budget, time). A matrix simplifies "as-produc