The Regulations on the Management of On-Site Inspections in Drug Registration was issued on May.23, 2008. It is formulated in order to regulate drug production and ensure the quality of on-site inspections in drug registration.
- Local Title:药品注册现场核查管理规定
- Country/Region:Chinese Mainland
- Competent Authority: Former China Food and Drug Administration (CFDA)
- Type:Regulation
- Status:In force
- Release Date:2008-05-23
- Implementation Date:2008-05-23