- An introduction to medical device management policies in China
- A summary of latest updates of medical device regulations
- New submission and approval process for medical device registration
- Practical advice on how to register the medical device in China
- The potential cost and duration of CFDA registration
- Specific requirements for classification determination
- Time: 18 June 2015, thursday , European 2:30-3:30 p.m. (GMT), American 8:30-9:30 a.m. (GMT-5), Asian 9:30-10:30 p.m. (GMT+8),
- Presentation Focus: Updates of CFDA Registration of Medical Device and IVDs in China
- Presenter: Mr Michael Petersen
- Registration fee: Free of charge;
Michael Petersen | 上官福调
Senior Consultant of Medical Device Legislation Compliance Department of CIRS
Mr. Michael Petersen is a Senior Consultant in the Medical Device Legislation Compliance Department of CIRS, he gained his master degree (Biomedical Engineer) from University of Columbia-Missouri in 2010. Michael has an extensive background in China medical device regulatory activities by developing compliance procedures for medical device registration in CFDA, compliance procedures for the entry of medical device and formulated technical methods for the regulatory risk management in China. He is as well as focused on the tracking and update of CFDA medical device regulations, deliver newsletter and significant info to clients.
- Manufacturers and distributors who export medical device or IVDs to China;
- Regulatory affairs specialist - healthcare;
- Quality control professionals
How to Register
After online registration, you will receive a link one day and one hour before the webinar starts. By clicking that link, you shall be able to join our webinar automaticallyNote: To attend this seminar, there is no need to call dial-in telephone number to access audio
Please note that space is limited.
Contact Us
- Ms. Elaine Lyu Elaine@cirs-group.com
Tel: +86-571 8720 6559 | Fax: +86-571 8720 6533