November 4, 2020
Pharmaceuticals and Medical Devices Agency
Purpose
Globalization of research and development, manufacturing and marketing of medical products has progressed, and cooperation in regulatory activities amongst regulatory agencies has become inevitably important. As the Asian region becomes significant in the area of clinical development and manufacturing of medical products today, PMDA strives to strengthen the collaborative relationship with the Asian regulatory agencies.
This is the joint conference with an aim to enhance Vietnam and Japan’s mutual understanding of regulatory systems to pursue more effective and efficient pharmaceutical regulations.
This symposium will offer presentations with our latest information and discussions from the pharmaceutical regulatory perspective in the area of pharmaceuticals review process, GMP inspection and E-labeling.
Host
Pharmaceuticals and Medical Devices Agency (PMDA)
The Drug Administration Department of Vietnam (DAV)
Support
Japan Pharmaceutical Manufacturers Association (JPMA)
The Japanese Chamber of Commerce and Industry in Vietnam (JCCI), Japanese Pharmaceutical Association in Vietnam (JPAV)
1. Date
1 Dec, 2020 (Tuesday)
2. Venue
The symposium will be held by virtual (Zoom).
Participants will receive the link by email.
3. Registration
- There is no registration fee for this symposium.
- Please register through the following website.
- Registration will be closed on 26th, Nov, 2020 (Thursday) or when the number of participants reaches the prearranged capacity.
- Please ask International Affairs Committee, JPMA about registration.
4. Interpretation
Simultaneous interpretation (Vietnamese-Japanese/Japanese-Vietnamese)