If you are a medical device manufacturer interested in the Chinese market, you are cordially invited to join the last webinar of the Cisema Webinar Series this year.
In the first webinar of the series, on March 4, 2021, we were delighted to share a basic understanding of the medical device registration process in China and have an interactive session with our participants.
In our second webinar, on June 8, 2021, our Cisema experts informed you about the latest regulatory changes in China, including Order 739, device lifetime, UDI, MAH system, and real-world data.
In our third webinar, on September 15, 2021, we have addressed the available entry pathways for medical devices and IVDs as an alternative to the standard NMPA registration pathway.
If you missed any of these webinars, feel free to let us know if you are interested to watch the replay. Watching the replays will equip you with a basic understanding of the registration process and recent hot topics.
In the upcoming webinar, our Cisema experts will be informing you about PMS requirements in China. Details as follows:
Thursday, December 2, 2021 – 10:00 CET – PMS, QMS, IVD and other hot topics
- Post-market surveillance: adverse events, recalls and periodic reporting
- Quality management system according to China requirements
- Latest updates for IVD registration
- Medical software and robotics products: Latest updates
- Latest status of Order 739 and implementing regulations and standards
Register here to keep up with the fast-changing regulatory environment in China.
You are encouraged to ask questions in our live webinars. Should you be in a different time zone, you are invited to register for the webinar series and watch the replay any time.
Contact Cisema if you have any questions.