Harmonizing VMPs Across Multiple Pharma Manufacturing Sites: Global Alignment & Regulatory Best Practices Harmonizing Validation Master Plans Across Multiple Pharma Sites As pharmaceutical companies scale operations across different regions, the need for a harmonized Validation Master Plan (VMP) becomes essential. A multi-site validation strategy ensures consistency, regulatory compliance, and efficient oversight across facilities. This article provides a detailed, action-oriented framework for standardizing VMPs across multiple manufacturing sites, while accommodating local regulatory variations and operational nuances. We also explore real-world examples and common pitfalls. 1. Why Multi-Site VMP Harmonization Matters Ensures global GMP compliance under ICH Q10 and FDA expectations Streamlines…