The Regulations on Drug Research Experiment Records (Interim) was passed by National Medical Products Administration (NMPA) on Jan. 3, 2000. It is formulated in order to strengthen drug research supervision and ensure drug research quality.
- Local Title:药品研究实验记录暂行规定
- Country/Region:Chinese Mainland
- Competent Authority: National Medical Products Administration (NMPA)
- Type:Regulation
- Status:In force
- Release Date:2000-01-03
- Implementation Date:2000-01-03