GMP, as part of the quality management system, is basic requirements of production and quality control of drugs, to ensure the products are manufactured in accordance with the registration requirements, and are suitable for their intended use, by minimizing the risks of contamination, cross-contamination, and mixups or errors in manufacturing process.
- Local Title:药品生产质量管理规范（2010年修订）
- Country/Region:Chinese Mainland
- Competent Authority: Chinese Pharmacopoeia Commission
- Status:In force
- Release Date:2011-01-17
- Implementation Date:2011-03-01