The Validation Master Plan (VMP) is a strategic document that guides all validation activities of a manufacturing facility to ensure consistent product quality and compliance with quality standards. As an essential element of a company's quality commitment, the VMP ensures that products and processes are systematically validated. It supports consistency and control in production, minimizes risks, and ensures regulatory compliance through detailed documentation and alignment with current regulations. Additionally, the VMP optimizes resource utilization and provides clear instructions for error minimization. It must comply with applicable regulatory requirements, such as those from the FDA and the EU. In general, the VMP establishes a company's validation strategy and defines and documents the intentions, responsibilities, approaches, and key aspects of a validation program.