The CIMDR has successfully concluded. Let’s review the highlights of CCRC booth

CIMDR Successfully Concluded

On Mar 4, 2023, the 13th China International Medical Device Regulatory Forum (CIMDR) hosted by China Center for Food and Drug International Exchange came to a successful conclusion in Fuzhou, Fujian Province.

The theme of the 13 CIMDR is “Improving Innovation System, Advancing Scientific Regulation, and Protecting & Promoting Public Health”, which covers the main points of the current medical device regulation work. In this CIMRD, the current regulations on medical device supervision and regulation were deeply analyzed and interpreted by professionals from the Department of Medical Device Registration, Department of Medical Device Regulation, Department of Science, Technology and International Cooperation, Center for Medical Device Evaluation, Center for Medical Device Standardization Administration, as well as other departments and affiliated organizations of the National Medical Products Administration.
Besides, representatives and experts from many countries and regions were invited, who have exchanged the latest measures and progress on regulations and supervision of medical devices.

 

Highlights of CCRC Booth

 

Providing Professional Speeches

We are happy to share with you that CCRC had prepared speeches on the themes of “Considerations and Challenges on the Implementation of Multi-Regional Medical Device Clinical Trials” and “Clinical Evaluation Pathway Selection in China for Medical Devices Approved in Europe and America – Types of Overseas Data that Can be Used”, which received overwhelming positive feedbacks from the visitors.

 

We look forward to seeing you at CIMDR next year!

As a CRO focusing on medical device technology, CCRC is committed to providing customers with one-stop clinical trial services for the whole lifecycle of medical devices. Except for accelerating the project process by working efficiently while ensuring high quality, CCRC is also actively implementing the Regulations on the Supervision and Administration of Medical Devices and will continue in focusing each and every detail during the service, and do our part to ensure the safety of the medical devices to be used.

CCRC sincerely thanks all CIMDR audience for your support. See you next year!