International Activities

FY2025 (April 2025 - March 2026)

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Seminars (open to all regulators)

Contents	Date Report
Pediatric Review	June 9 to 12 Report
GMP(Good Manufacturing Practice) Inspection	September 17 to 19 Report
Herbal Medicine Review	November 18 to 21 Report
Pharmaceuticals Review	December 9 to 11 Report
Multi-Regional Clinical Trial(MRCT)/ Good Clinical Practice (GCP) Inspection ^{(Note 1)}	January 27 to 30 Report
Pharmacovigilance^{(Note 1)}	February 25 to 27 Report

^{(Note 1)} APEC-SCSC-RHSC CoE Workshop

Other Seminars (for specific members)

Contents	Date Report
PMDA-ATC Safety Reporting System of Clinical Trial Webinar 2025 （for NPRA, Malaysia）	April 30 Report
ASEAN-Japan Medical Devices Regulatory Seminar 2025 (for regulatory authority officials in ASEAN Member States)	May 15 to 16 Report
PMDA-ATC SaMD Webinar 2025 （for Thai FDA, Thailand）	May 27 Report
PMDA-ATC Over-The-Counter (OTC) Drugs Seminar 2025 （for NPRA, Malaysia）	June 10 to 12 Report
Review of Cell therapy and Gene therapy products (CGTPs) (for South-East Asian Countries)	July 15 to 17 Report
Pharmaceutical Review (for ASEAN member states)	October 7 to 10 Report
Medical Devices (for ASEAN member states)	October 17 Report
PMDA-ATC Clinical Trial Webinar 2026 (for FDA Philippines, Philippines)	February 5 Report