The Pharmaceutical Good Manufacturing Practice (GMP) Certification Inspection and Evaluation Standards was issued on Oct.24, 2007. It is formulated to evaluate and ensure that drug manufacturers comply with Good Manufacturing Practice (GMP) requirements. This standard covers requirements for pharmaceutical processes, equipment, production environment, drug quality control, etc. to ensure that the drugs produced meet high standards in terms of quality and safety.
- Local Title:药品GMP认证检查评定标准
- Country/Region:Chinese Mainland
- Competent Authority: Former China Food and Drug Administration (CFDA)
- Type:Regulation
- Status:In force
- Release Date:2007-10-24
- Implementation Date:2007-10-24