Welcome to register for the 11th China International Medical Device Regulatory Forum

  • 2020-08-10

Date: November 17-20, 2020
Venue: Fuzhou Strait International Conference & Exhibition Center • China
Registration deadline: October 16, 2020
Contact: Mr./Ms. Liang
Tel:(010)85659462   E-mail: liangyb@camdi.org
Forum details:
I. Schedule and contents
November 17: all-day registration
November 18 (all-day) & November 20 (afternoon): plenary assembly
Opening ceremony to publicize and explain newly released relevant laws and regulations, latest policies of medical device evaluation and approval reform, and implement supporting department rules and regulations - relevant leaders of regulatory authorities for medical devices
Introduction of international supervision regulations on medical devices, technological means and medical device standards - regulatory authorities for medical devices, technical institutions, medical device standard organizations and industry experts from various countries.
November 19 (all-day) & November 20 (afternoon): sub-forum
1. Medical device innovative technology and product forum
2. Medical devices clinical evaluation forum
3. Medical device regulatory science forum
4. Medical device standards and UDI implementation forum
5. Medical device biological evaluation forum
6. Medical device post-marketing review and risk management forum
7. Medical device network security forum
8. Artificial intelligence forum
9. Orthopedic, dental and surgical devices forum (including contents on 3D printing and customized products)
10. In vitro diagnostic devices (including companion diagnostic agents) forum
11. Drug-device combination products forum
12. Medical imaging devices forum
13. Medical polymer products and consumables forum
14. Cardio-cerebral system devices forum
15. Ophthalmic and optometry devices forum
16. RWE & real-world data forum
17. Emergency management and anti-epidemic protective products forum (including topic on body temperature management)
In order to further promote the development of innovative medical devices, improve development quality, enhance risk governance and responsibility implementation, and encourage the development of small and micro enterprises of medical devices, parallel sessions such as "Medical Device Administrator (MD50)" and "Legal Affairs Personnel Development" will be held at the time of forum to explore the scientific and legalized supervision of medical devices and new technologies of innovative medical devices. Representatives from the medical device field and relevant sectors are welcomed to attend the sessions.
(See the Chinese website for more information)