Suggested Reading
- Rules for Medical Device Nomenclature( April 1, 2016)
- Provisions for the Supervision and Administration of Drug Manufacturing(July 1, 2020)
- Provisions for Drug Registration(July 1, 2020)
- 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 Instructions and Labels of Medical Devices(October 1, 2014)
- 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)
- Review Guideline of Animal Studies for Medical DeviceRegistration: Part 1 Decision Principles(2021Revision)