Suggested Reading
- Provisions for Adverse Drug Reaction Reporting and Monitoring(May 4, 2011)
- Regulations for the Administration of Overseas Inspection of Pharmaceutical & Medical Devices (December 26, 2018)
- Provisions for the Supervision and Administration of Drug Manufacturing(July 1, 2020)
- Drug Administration Law of the People's Republic of China(December 1, 2019)
- Provisions for Supervision and Administration of Medical Device Manufacturing(May 1, 2022)
- Provisions for Supervision and Administration of Medical Device Distribution(May 1, 2022)
- Provisions for Supervision of Drug Distribution(May 1, 2007)
- Provisions for Drug Insert Sheets and Labels(June 1, 2006)
- Provisions for Drug Registration(July 1, 2020)
- Provisions for Drug Importation(January 1, 2004)
- Provisions for Administration of Medical Device Recall(May 1, 2017)
- Provisions for Instructions and Labels of Medical Devices(October 1, 2014)