About this document
Quality Audit Process in GMP Compliance by rana mokbel is a document available to read on EtoBox.
This document discusses quality auditing in the pharmaceutical industry. It defines quality auditing and outlines its purpose to systematically examine quality assurance systems and ensure compliance with good manufacturing practices. The key points covered include: - Components of quality auditing include personnel, contamination control, sanitation, premises, documentation, and audits. - Audits can be internal or external, and are conducted to build confidence and monitor suppliers and distributors. - E
- Author
- rana mokbel
- Language
- EN