Standard Operating Procedure (SOP) for Validation of Deviation Management in Analytical Laboratory

Document ID: SOP-TEMP-001 (Example) Revision Number: 01 (Example) Effective Date: 2024-03-08 (Example) Author: [Your Name/Department] Approver: [QA/QC Department] 1. Purpose: This SOP outlines the procedure for validating the deviation management system within a drugs testing and analytical laboratory. This validation aims to ensure the system effectively identifies, documents, investigates, and resolves deviations from established procedures, standards, and quality requirements, maintaining […]