- Seminars (open to all regulators)
| Contents | Date Report |
|---|---|
| Pediatric Review (Note 1) | July 10 to 13 Report |
| Quality Control (Herbal Medicine) | August 22 to 24 Report |
| Good Registration Management (GRM) | September 6 to 8 |
| Pharmaceuticals Review | September 26 to 28 Report |
| Medical Devices Review (Note 2) | November 14 to 16 Report |
| Medical Devices Review (PMDA-ATC Medical Devices Seminar 2023) | December 5 to 7 Report |
| Multi-Regional Clinical Trial (MRCT) (Note 2), (Note 3) | January 23 to 26 Report |
| Good Manufacturing Practice (GMP) | February 6 to 7 Report |
| Pharmacovigilance (Note 2) | February 26 to 29 Report |
(Note 1) Joint Seminar with U.S.FDA
(Note 2) APEC RHSC CoE Workshop
(Note 3) Collaboration with National Cancer Center Japan
Other Seminars (for specific members)
| Contents | Date Report |
|---|---|
| Pharmaceutical Review (for DAV Vietnam) |
April 21 Report |
| Risk Management Plan (RMP) (for regulatory authority officials in ASEAN Member States) |
May 25 to 26 Report |
| Good Manufacturing Practice (GMP) (for CDSCO, India) |
May 29 Report |
| Regenerative Medicinal Products Review (for CDSCO, India) |
June 28 Report |
| Pharmaceuticals Review (for JICA (Note 1) trainees) |
July 20 to 21 and 24 to 26 Report |
| First in Human studies of Regenerative Medical Products (for NPRA, Malaysia) |
July 26 Report |
| Approval and registration system, Orphan drug (for SFDA, Saudi Arabia) |
November 28 Report |
| Medical Devices Review (PMDA-ATC/AMDC Medical Devices Webinar 2023) (for AMDC member states) |
December 4 Report |
| Pharmaceutical Review, Pharmacovigilance (for FDA Philippines, Philippines) |
December 14 to 15 Report |
(Note 1) JICA : Japan International Cooperation Agency