- Seminars (open to all regulators)
| Contents | Date Report |
|---|---|
| Pediatric Review (Note 1) | July 22 to 25 Report |
| Good Registration Management (GRM)) | September 3 to 5 |
| GMP(Good Manufacturing Practice) Inspection | October 8 to 10 Report |
| Medical Devices Review and Post-marketing Safety (Note 2) | October 29 to 30 Report |
| Medical Devices Review | October 31 to November 1 Report |
| Herbal Medicine Review | November 12 to 15 Report |
| Pharmaceuticals Review | December 10 to 12 Report |
| Multi-Regional Clinical Trial(MRCT)/ Good Clinical Practice (GCP) Inspection (Note 2) | January 21 to 24 Report |
| Pharmacovigilance | February 26 to 28 Report |
(Note 1) Joint Seminar with U.S.FDA
(Note 2) APEC-SCSC-RHSC CoE Workshop
- Other Seminars (for specific members)
| Contents | Date Report |
|---|---|
| Pharmaceuticals Review (for PPWG member states) |
June 11 to 14 Report |
| Review of Cell therapy and Gene therapy products (for PPWG member states) |
June 27 to 28 Report |
| Generic Drugs Review (for NPRA, Malaysia) |
July 11 Report |
| GCP Inspection (for NPRA, Malaysia) |
August 26 Report |
| Radiopharmaceuticals Review (for FDA Philippines, Philippines) |
November 19 Report |
| Medical Gases and Pharmacovigilance (for Thai FDA, Thailand) |
February 4 Report |