Free Webinar: How to Access the Chinese Medical Device Market（English/Korean）

China’s medical device market is rapidly growing these years, China offers numerous opportunities for foreign healthcare related companies but understanding the practicalities of accessing the market is not simple. CIRS is glad to host this webinar to present you the latest regulatory updates and the practical advices on how to access Chinese medical device market.

In this webinar, you will learn about

The current situation of Chinese medical device market;
The regulatory structure of Chinese medical devices market;
The latest changes by the CFDA in the product registration, clinical trials and GMP;
Opportunities and challenges for foreign companies in new regulatory environment;
Practical solutions for overseas medical devices to access the Chinese market;

Time and Schedule

Webinar 1 (English)

Time: 30 Aug. 2016, Tuesday, PM 5:00-6:00 (GMT+8 China), AM 9:00-10:00（GMT)
Presenter: Ms Elaine Lyu Senior Consultant of Medical Device Legislation Compliance
Registration fee: Free of charge

Webinar 2 (Korean)

Time: 30 Sep. 2016, Tuesday, PM 2:00-3:00 (GMT+8 China), PM 3:00-4:00 (GMT+9 Korea)
Presenter: Mr Jason Zhuo Senior Consultant of Medical Device Legislation Compliance
Registration fee: Free of charge;

About the Presenter

Elaine Lyu | 吕烨

Senior Consultant of Medical Device Legislation Compliance
Ms. Elaine Lyu is a Senior Consultant in the Medical Device Legislation Compliance Department of CIRS, she gained her master degree (Advancing Practice) from University of Worcester. Elaine has extensive background in China medical device regulatory activities by developing compliance procedures for medical device registration in CFDA, and she is the most professional consultant in assisting imported medical devices access in Chinese market. Moreover, she focuses on tracking and update of CFDA medical device regulations, share the most relevant newsletter and significant info with the clients.

Jason Zhuo| 禚新杰

Senior Consultant of Medical Device Legislation Compliance
Mr. Jason Zhuo is a Senior Consultant in the Medical Device Legislation Compliance Department of CIRS, he is responsible for helping foreign companies comply with the CFDA regulations. He has provided solution proposals for many Korean companies planning to export medical device products to China market.

Who Shall Attend

Manufacturers and distributors who export medical device or IVDs to China;
Regulatory affairs specialist - healthcare;
Quality control professionals

How to Register

Click the link below to register
Webinar 1(English) :
https://cirs.webex.com.cn/cirs-en/onstage/g.php?MTID=e336d9ef11fb798f74f5844433018339c

Webinar 2 (Korean) :
https://cirs.webex.com.cn/cirs-en/onstage/g.php?MTID=e4e155f72bd53c7341aaf3d1f377875fe

Please consider your time zone and language.

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. Please note that space is strictly limited to a maximum of 100 attendees.

Contact Us

Hangzhou CIRS Co. Ltd (CIRS China) | Beijing CIRS Tech Co. Ltd (CIRS Beijing)

Ms. Elaine Lyu, Elaine@cirs-group.com
Mr. Michael Petersen, Michael@cirs-group.com
Mr. Jason Zhuo, Zxj@cirs-group.com
Tel: +86-571 8720 6559 | Fax: +86-571 8720 6533

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