Navigating the Regulatory Process to Expedite Your Product Entering into China Market
The webinar, “Navigating the Regulatory Process to Expedite Your Product Entering into China Market” cosponsored by CCRC and Dinova Israel Incubator was successfully held on Dec 19, 2022.
Highlights Overview
Opening Address
CCRC General Manager Julia
Introduction of Dinova Israel Incubator
Yaniv, Chief Operating Officer,
Dinova Israel Incubator
Overview of CCRC
Shawn, Sr. Director,
Strategic Development of CCRC
Clinical Evaluation Pathway Selection in China for Medical Devices Approved in Europe and America –
Types of Overseas Data that Can be Used
Sophie, Associated Director of Regulatory Affair
The registration of overseas approved medical devices in China –
proper use of overseas clinical data
Yanfang, Medical Director
Q&A
To help overseas enterprises learn the details of medical device registration in China, an open discussion session was left in this seminar. In response to the questions from online audience, the speakers provided professional answers in their respective fields, and had in-depth discussions and message exchanges, which benefited the audience a lot.
As a global CRO company focusing on medical devices, CCRC has rich experiences in helping local devices going overseas and overseas devices entering China. This seminar is the first one held by CCRC for overseas customers. In the future, CCRC will be more active in the international industry exchange activities. Thanks for your attention, and we are looking forward to seeing you next time!
