Dear European Stakeholders,
In China , Medical devices imported from Overseas need to get CFDA registration and fulfil China medical devices regulations and standards. To help the European industries better understand updated Medical Devices market access requirements and what kind of standards can industry apply, SESEC IV will organize a webinar on “Registration Rules and Standards Used for Medical Devices Exporting to China”
Detailed information is as follows.
SESEC IV Webinar 02
Topic: “Registration Rules and Standards Used for Medical Devices Exporting to China“.
Time and Date: 9:30- 11:00 am Brussel time, Friday, 30 November 2018
Presenters: Miss FAN Bo and Dr. Betty Xu (see the attached CV of the speakers)
Main contents: the most recent development of Registration rules and standards used for medical devices in China market, including the organization changes of CFDA and the rules and standards policies of CFDA.
Language： Chinese presentation with alternative English interpretations.
Presentation Download: Registration process of imported medical Devices in China-Nov.2018
Please register your participants via following links. https://attendee.gotowebinar.com/register/7443682020170359809
Thank you and best regards
Dr. Betty XU
Seconded European Standardization Expert in China (SESEC)
A project co-funded by CEN, CENELEC, ETSI, EC and EFTA
Room 1005,The Oriental Place, #9 East Dongfang Road,
Chaoyang, Beijing, 100106, P R China
Phone: +86 10 85275366-802
Fax: +86 10 8527 6363
Mobile:+86 185 118 20197