Free Webinar: China Medical Device Master File (MFs) Registration System Online Seminar – Empowering Global Enterprises for Efficient Market Access in China - Events - Medical Devices

China's Market, Global Opportunity: Unlocking the New Key to Compliant Medical Device Market Access

As one of the world's most promising medical device markets, China is opening its doors wider to global innovative products through continuous regulatory innovations by the National Medical Products Administration (NMPA). Among these, the Medical Device Master File (MFs) registration system is a key initiative. It provides an excellent pathway for global suppliers of raw materials, critical components, software, and manufacturing processes to protect their intellectual property and efficiently support their Chinese clients in completing product registration.

However, for overseas enterprises, geographical distance, language barriers, and unfamiliarity with NMPA requirements pose challenges alongside the benefits of MFs registration: How to ensure technical documentation fully complies with requirements? How to efficiently complete the online registration platform operations? How to communicate effectively with Chinese regulators and partners?

To help global medical device industry chain enterprises accurately grasp this system, we are hosting this specialized online seminar. This webinar will provide an in-depth analysis of the strategy, practical operations, and case studies related to MFs registration, offering clear guidance for the smooth entry of your products into the Chinese market.

Time

Language	Date	Time (Beijing Time,GMT+8)	Speaker
English	November 20 2025	17:00 – 18:00 pm	Yolanda YAN

Registration Fee

Free

Main Contents

- Introduction to the NMPA Medical Device Master File (MFs) System

- Key Operational Points for NMPA MFs Submission

- Case Studies

Speaker

Yolanda YAN, BD Manager

Ms. Yolanda YAN is the BD Manager of 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, helped many overseas medical equipment products successfully enter the Chinese market.

Registration

Registration link: https://us06web.zoom.us/webinar/register/WN_zL0uqqyhT_euf6RwRJ1Flg

Note: You will receive emails with a link one day and 15 minutes 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 500 attendees.

System Requirement

On PC: Before joining a Zoom meeting on a computer, you can download the Zoom app from Download Center. Otherwise, you will be prompted to download and install Zoom when you click a join link.

On Mobile Service: Zoom mobile app downloaded from the App store or the Google Play Store

If you need further assistance about joining the webinar, please click here to Zoom Help Center.

Contact us
Chemical Inspection & Regulation Service (CIRS)
Addr: 11/F., Building 1, Dongguan Hi-Tech Park, 288 Qiuyi Road, Binjiang District, Hangzhou 310052, China
TEL: +86 571 8720 6574
Email: service@cirs-group.com

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+86 571 8720 6559 （GMT+8 8:30~17:00）

md@cirs-group.com

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