To further standardize the electronic supervision of drugs, improve work efficiency and fulfill the tasks under the Twelfth Five-Year Plan for National Drug Safety, the State Food and Drug Administration (SFDA) organized the drafting and recently issued the Guiding Opinions on Electronic Supervision of Drugs based on related regulations and the Technical Guidance for Electronic Supervision of Drugs.
- SFDA Deputy Commissioner Bian Zhenjia meets Deputy Commissioner of US FDA
- SFDA issues notice on standardizing the labels and packaging marks of foreign medical devices
- SFDA Commissioner Yin Li meets the delegation from Center for Genetic Engineering and Biotechnology of Cuba
- SFDA issues the Guide for the Application and Review of Children's Cosmetics
- SFDA issues Guiding Opinions on Electronic Supervision of Drugs
- SFDA releases 2011 Annual Report on Drug Registration Approval
- SFDA Commissioner Yin Li meets the delegation of Roszdravnadzor
- New version of EN ISO 14971:2012 was published
- New version of EN ISO 13485:2012 was published
- Transition from ISO 19011:2002 to a new version ISO 19011:2011