Managing Documentation Deviations in Process Validation Protocols
Managing Documentation Deviations in Process Validation Protocols Managing Documentation Deviations in Process Validation Protocols Introduction: In the pharmaceutical industry, process validation is a critical component of ensuring product quality and compliance with regulatory standards. It involves a series of documented procedures and protocols designed to confirm that a manufacturing process consistently produces a product meeting…
Read More “Managing Documentation Deviations in Process Validation Protocols” »