July 23, 2020 @ 11:00 am – 12:00 pm

The China IVD market has seen record growth recently and will continue to be an important market with the growing threat of cancer and COVID-19. Join us on Thursday, July 23 from 11:00 a.m. – 12:00 p.m. EDT for the free webinar: China IVD Registration Pitfalls and COVID-19 Test Kit Updates. Attendees will receive comprehensive IVD guidance based on NMPA’s public training programs, as well as the latest guidance relating to COVID-19 test kits. Don’t miss this opportunity to learn more about NMPA’s requirements for IVD product registration! Topics Covered:
- What are the key regulations for IVD/CDx in China?
- How to determine the registration units when applying for NMPA approval
- How to prepare the registration documents to meet the specific requirements described in regulation guidelines
- What are the pitfalls in the registration process?
- What are the key clinical pathways?
- What is the current status of NMPA approved COVID-19 detection kits?
- What are the clinical trial requirements on COVID-19 detection kits?
Details
- Date:
- July 23, 2020
- Time:
-
11:00 am – 12:00 pm
- Website:
- https://eur04.safelinks.protection.outlook.com/?url=httpschinameddevice.us17.list-manage.comtrackclicku4570e530cd0985e087bfc7971id1f88001eade2937493e62&data=0201e46f4e40cbfb4f15450908d82d8742ab84df9e7fe9f640afb435aaaaaaaaaaaa10637309406244470153&sdata=WNCrxRmBvK5Ult4FOLYnxmYOe7vWosfBH1hGkkMQ&reserved=0