Standard Operating Procedure For Revalidation Procedure

Purpose: This document outlines the procedure for revalidating equipment, processes, and systems to ensure continued compliance with established standards and regulatory requirements. 1. Revalidation Categories 1.1. Process Revalidation: Generally, process revalidation (excluding sterile/aseptic processes) is not routinely performed. Validated status is maintained through the change control system. Revalidation outside of change control is considered only if there are repeated or […]

Tips to Develop Equipment Cleaning Procedure in Pharmaceuticals

Quality management in pharmaceuticals is a critical factor to both the pharmaceutical companies and the public at large Through this article, the following tips will be crucial to developing the equipment cleaning procedure for use in the pharmaceutical industries: Cleanliness of equipment in the pharmaceutical manufacturing processes is very important so as to meet quality standards, minimize risks from contamination […]