The Supplementary Provisions for Registration and Approval of Non-prescription Drugs was passed by Former China Food and Drug Administration (CFDA) on Mar. 16, 2004. It sets the scope, application, declaration material, clinical research, application of imported non-prescription drugs for registration and approval of non-prescription drugs in China.
- Local Title:非处方药注册审批补充规定
- Country/Region:Chinese Mainland
- Competent Authority: Former China Food and Drug Administration (CFDA)
- Type:Regulation
- Status:In force
- Release Date:2004-03-16
- Implementation Date:2004-03-16