SESEC IV Webinar No 2 :“Registration Rules and Standards Used for Medical Devices Exporting to China”

Date: 11/30/2018
Time: 9:30 am  to  11:00 am
Location:

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.

 

 

Please register your participants via following links. https://attendee.gotowebinar.com/register/7443682020170359809

 

Thank you and best regards

 

Betty

 

 

Dr. Betty XU

Seconded European Standardization Expert in China (SESEC)

A project co-funded by CEN, CENELEC, ETSI, EC and EFTA

 

Beijing Office:

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

E-mail: betty.xu@sesec.eu

Website: www.sesec.eu

 

Betty XU_ Bio _2018_11 Resume of Bo Fan(1)