In this webinar we will give a comprehensive report on new medical device regulations in 2018, practical advices for corporates to adapt to new regulation and possible policy trend in 2019.
Topic Covered
- Summary of new medical device regulations in 2018- Implementation of China medical device marketing authorization holders (MAH)
- New medical device classification catalogue and clinical trial exempt catalogue
- Practical tips on China medical device compliance under the new regulations
- Prospect of China medical device supervision trends in 2019
Time and Schedule
Language | Date | Time (Beijing Time, GMT+8) | Speaker |
English | 21 January 2019 | 16:50-17:35 | Miss Shuo Wang |
Registration Fee
Free
About the Presenter
Ms. Shuo Wang, Medical Device Specialist, CIRS GROUPMs. Shuo Wang completed her master degree in the biology program of Leiden University. She has extensive background in life science industry, after joining CIRS GROUP, she focuses on the medical device market and providing professional medical device regulatory compliance support for oversea corporations.
Who Shall Attend
• Manufacturers and distributors who wish to enter China medical device/ IVD market;• Regulatory affairs specialist - Healthcare;
• QA and QC professionals
How to Register
Click the link below to register
Note: You will receive a link one day before the webinar starts. By clicking that link, you shall be able to join our webinar automatically. Please note that space is strictly limited to a maximum of 100 attendees.Contact Us
Hangzhou, ChinaHangzhou REACH Technology Group Co., Ltd. (CIRS Group)
Addr: 11/F., Building 1, Dongguan Hi-Tech Park, 288 Qiuyi Road, Binjiang District, Hangzhou 310052, China
• Ms. Shuo Wang, Wangshuo@cirs-group.com
Tel: +86-571 8720 6559 | Fax: +86-571 8720 6533