This webinar will introduce the content of China's Medical Device regulatory updates in 2020 and the regulatory requirements for the registration of imported medical devices in China.
- 2020 China Medical Device Regulation Update
- Registration requirements for the transfer of imported medical devices to domestic products
- UDI implementation in China
- Chinese medical device regulations and registration requirements
- Imported medical device registration data requirements
Time: 2021.2.23 PM 14:00-15:00 (Korea Time)
2021.2.23 PM 13:00-14:00 (Beijing Time)
Presenter: Dayoung Lee
Webinar Fee: Free
Organization company: CIRS Group Korea Co., Ltd.
Jinwoo Cho Team Leader
Lee Da-Young Senior Consultant
How to participate:
Please click the link below to attend the meeting directly：
Please download and fill in the following application form, and then send it to our contact so that we can notify you before the meeting
Ms. Dayoung Lee, junior consultant, CIRS Group Korea
Ms. Dayoung Lee is the junior consultant of the Medical Device team of CIRS Group Korea. She Complete her bachelor's degree in major of BME (Biomedical Engineering), Korea. She specializes in the medical device market and provides professional consulting services of regulation compliance to overseas companies, helped many overseas medical equipment products successfully enter the Chinese market.
CIRS Group introduction
CIRS Group is a professional product regulatory compliance and technical consulting service firm. With its headquarters based in Hangzhou of China and branch offices and laboratories located in Ireland, US, UK, Korea, Beijing, Nanjing, Ningbo and Hong Kong.
The CIRS Medical Device Business Unit has a long-term commitment in global medical device technology, laws and regulations and industry police. With its professional and technical experiences, multiple resources and global network, CIRS assist domestic and oversea medical device enterprises with a comprehensive service chain and one-stop solution in medical devices regulation and technical consulting service, including medical devices registration and approval, clinical trials, quality management system, manufacturing and distributing license, technology consulting, laws and regulations training. We are dedicated to help medical devices enterprises gaining competitive advantage by reducing business risks associations with regulatory affairs and removing barrier to entry