Scheduled Date
August 26-28, 2026
Venue Location
Taipei, Chinese Taipei
About Workshop
Target Audience
Co-Organizers
Contact Information
The 2026 APEC Good Registration Management (GRM) Regulatory Science Center of Excellence (CoE) Workshop focuses on training and education related to AI-driven regulatory review and reliance in the generic drug lifecycle.
Through this workshop, participants are expected to strengthen their understanding of international practices and enhance their ability to apply the principles of Good Review Practices (GRevP) and Good Submission Practices (GSubP). The program aims to promote a more efficient registration process for medical products across the APEC region.
Schedule & Venue
Through this workshop, participants are expected to strengthen their understanding of international practices and enhance their ability to apply the principles of Good Review Practices (GRevP) and Good Submission Practices (GSubP). The program aims to promote a more efficient registration process for medical products across the APEC region.
August 26-28, 2026
Chang Yung-Fa Foundation International Convention Center
Address: No.11, Zhongshan South Road, Taipei City
Website: Click Here
- Regulatory professionals from authorities with hands-on experience in the management of regulatory reviews.
- Regulatory professionals from Industries with hands-on experience in the management of regulatory submissions.
- Academia who are interested in learning GRevP or GSubP guidelines.
- Professional bodies who are actively involved in training.
- Hybrid Training on Day 1 and Day 3, with limited on-line participation prioritized for overseas attendees.
- In-Person Session on Day 2, featuring interactive case studies and group discussions with overseas and TFDA reviewers, as well as industry representatives. In-person participants will also be invited to the Welcome Reception Dinner. Limited travel support for eligible regulatory authority participants may be available.
- Certificates will be awarded to participants who complete all three days of the workshop.
Please note that these are for reference only, and no promotional code is available.
Cosmos Hotel Taipei
Address: No. 43, Sec. 1, Zhongxiao W. Rd., Taipei City
Website: Click Here
OOD by check
Address: No. 12, Sec. 1, Hangzhou S. Rd., Taipei City
Website: Click Here
Address: No. 43, Sec. 1, Zhongxiao W. Rd., Taipei City
Website: Click Here
OOD by check
Address: No. 12, Sec. 1, Hangzhou S. Rd., Taipei City
Website: Click Here
Funding may be available for regulators from travel-eligible economies. Priority will be given to regulator representatives who are willing to share updates on drug review mechanisms in their economies during the workshop.
CoE Hosting Institution
Taiwan Food and Drug Administration
Ministry of Health and Welfare
The APEC Regulatory Harmonization Steering Committee
Pharmaceuticals and
Medical Devices Agency
Asia Partnership Conference of Pharmaceutical Associations
ITRI Secretariat at TFDAGRMCOE@gmail.com