- 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.
- In-person training.
- 3 days of plenary sessions designed with lectures, group discussions, and applied case studies for all attendees.
Funding for travel eligible economies may be available for regulators. Regulator representatives willing to share recent GRM implementation status in their member economies may be prioritized.
CoE Hosting Institution：Taiwan Food and Drug Administration (TFDA)
Contact Information：GRMCOE2025@gmail.com