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    Free Webinar: China Medical Device Regulation Overview and Update

    from CIRS by

    China's medical device regulation system started late and has a short development history, but it has developed very rapidly in recent years. In order to provide a better environment for medical devices industry and promote the development of China's medical device industry, many regulations and systems are constantly being revised and updated. Therefore, in response to the rapid changes in Chinese regulations, overseas medical device enterprises need to develop new compliance strategies.

    In this webinar, we will discuss the latest changes of China's medical device regulations which involves UDI, MAH, etc. and provide practical advices for overseas medical device enterprises to register and marketing in China under the new regulations. We hope it will help you build an overview of China's regulation and solve your problems.

    Topic covered

    - Overview of China medical device management

    - The latest update of China medical device regulation

    - Implementation progress of Medical Device Unique Identification (UDI) in China

    - Overview of China Medical Device Registration Electronic Declaration Information System (eRPS)

    - Amendments of Medical Device Supervision and Administration Regulations

    - Brief Analysis of MAH System of Medical Device industry in China

    - Practical advices on how to register a medical product in China

    Time and Schedule

    Language

    Date

    Time (Beijing Time, GMT+8)

    Speaker

    English

    5th December 2019

    17:00 – 18:00

    Yolanda YAN

    Registration Fee

    Free

    About the Presenter

    presenter Yolanda

    Ms. Yolanda YAN, Regulatory Affairs Consultant, CIRS Group

    Ms. Yolanda YAN is a consultant in the Medical Device Business Unit of CIRS Group. She Complete her master degree in the IMS major of IMT-BS (Telecom Ecole de Management), France. She specializes in the medical device market and provides professional consulting services of regulation compliance to overseas companies.

    Who Shall Attend

    ? Manufacturers and distributors who wish to enter China medical device/ IVD market;

    ? Regulatory affairs specialist - Healthcare;

    ? QA and QC professionals

    How to Register

    Click the link below to register

    Note: You will receive a link one day before the webinar starts. By clicking that link, you shall be able to join our webinar automatically. Please note that space is strictly limited to a maximum of 100 attendees.

    Contact Us

    Hangzhou REACH Technology Group Co., Ltd. (CIRS Group)

    · CIRS Group: 11/F., Building 1, Dongguan Hi-Tech Park, 288 Qiuyi Road, Binjiang District, Hangzhou 310052, China

    · CIRS Beijing: No. 7 West Block, Dacheng Plaza, 28 Xuanwumen Xidajie, Xicheng District, Beijing, China

    · Ms. Yolanda YAN, yolanda.yan@cirs-group.com or md@cirs-group.com

    Tel: +86-571 8720 6559 | Fax: +86-571 8720 6533

      

    We have launched a LinkedIn newsletter to keep you up to date on the latest developments across the chemical industry including food and FCMs and personal and home care.

    Contact Us
    +86 571 8720 6559 (GMT+8 8:30~17:00)
    Contact Us
    +86 571 8720 6559 (GMT+8 8:30~17:00)
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