Free Webinar: Specifically know how to determine the classification of medical devices in China

This webinar will focus on the guidance on how to determine the classification of medical devices in China and introduce devices those had been changed their classifications under the new regulations, as well as a very smart database system to be introduced to automatically classify your medical devices.
If you are a manufacturer or distributor involved in exporting medical device or IVDs to China, this webinar will provide you with very practical direction to classify your medical devices quite exactly and efficiently. Professional suggestions/opinion will also be given for your reference, based on our previous experiences.

Topics Covered

• An overview of CFDA regulations on the medical devices classification
• Specific requirements for classification determination
• A summary of latest classification change of some medical devices
• Practical advice on how to classify your medical devices in China
• Classification case study of some medical devices
• Easy direction to use China Medical Device Classification System (CMDCS)

Time and Schedule

• Time: 27^th Aug 2015, Thursday, European (GMT) 15:00-15:45, American (GMT-5) 10:00-10:45, Asian (GMT+8) 22:00-22:45
• Presentation Focus: specifically know how to determine the classification of medical devices in China
• Presenter: Mr. Michael Petersen
• Registration fee: Free of charge;

About the Presenter

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.

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. Windy Jin, Windy@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