Free Webinar: Latest Regulatory Updates on Medical Devices in China - Regulatory News - Medical Devices

This webinar will focus on the latest updates of medical device regulations in China and assess how those changes will impact the registration of medical devices and in vitro diagnostic reagents (IVDs) in China.

If you are a manufacturer or distributor involved in exporting medical device or IVDs to China, this webinar will provide you with necessary briefing on CFDA registration of medical devices and in-depth intelligence on how these regulatory updates affect your business. Professional suggestions/opinion will also be given for your reference, based on our previous experiences.

Topics Covered

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 and Schedule

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;

About the Presenter
Michael Petersen | 上官福調

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.

Who Shall Attend

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 automatically

Note: 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

11F Building 1, Dongguan Hi-Tech Park, 288 Qiuyi Road, Binjiang District, Hangzhou 310052, China
Tel: +86-571 8720 6559 | Fax: +86-571 8720 6533

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