Suggested Reading
- Provisions for Adverse Drug Reaction Reporting and Monitoring(May 4, 2011)
- Provisions for the Supervision and Administration of Drug Manufacturing(July 1, 2020)
- Provisions for Drug Insert Sheets and Labels(June 1, 2006)
- Provisions for Supervision of Drug Distribution(May 1, 2007)
- Provisions for Drug Importation(January 1, 2004)
- Provisions for Supervision and Administration of Online Drug Sales(December 1, 2022)
- Rules for Classification of Medical Devices (July 14, 2015)
- The Provisions for Registration and Filing of Cosmetics(May 1, 2021)
- Guidelines for the Use of Real-World Data in Clinical Evaluation of Medical Devices-Trial(Nov 24, 2020)
- Provisions for Supervision and Administration of Medical Device Manufacturing(May 1, 2022)
- Provisions for Administration of Medical Device Recall(May 1, 2017)
- Provisions for Supervision and Administration of Medical Device Distribution(May 1, 2022)