Analytical Method Transfer & Revalidation: Protocols, Risks & Audit Readiness Analytical Method Transfer & Revalidation in Pharma: Protocols, Risks & Audit Readiness In the pharmaceutical industry, the accurate and reproducible application of validated analytical methods across different laboratories is vital for product quality and regulatory compliance. Whether transferring a method from R&D to QC, between manufacturing sites, or to a contract testing lab, the method transfer process must follow defined protocols and ensure analytical equivalence. Similarly, method revalidation ensures that any changes impacting analytical parameters are re-assessed per current regulatory expectations. This in-depth guide covers analytical method transfer and revalidation…