Key Sections of a Pharma VMP: Content, Hierarchy & Regulatory Flow Understanding the Key Sections of a Pharma VMP: Content, Hierarchy & Regulatory Flow The Validation Master Plan (VMP) is the backbone of a pharmaceutical company’s qualification and validation activities. It is a high-level document that provides a structured plan, regulatory justification, and scope of validation for systems, facilities, equipment, processes, analytical methods, and utilities. Whether for a new facility, product launch, or lifecycle validation, a well-structured VMP ensures regulatory compliance and audit readiness. This guide offers a detailed breakdown of the essential components, hierarchical flow, and practical regulatory expectations…