News & Events

2017-05-18 Faster Process for Medical Devices Access to the Chinese Market

2017-05-12 CFDA Reconstruct the Medical Device Clinical Trial Policies in China

2017-05-12 CFDA’ s Oversea Medical Devices Inspections Upgraded

2017-04-19 CFDA adjusts some administrative approval procedures for medical devices

2017-04-19 The Statistics of Imported Class I Medical Device filing in China

2017-04-17 The Annual Report for China Medical Device Registration in 2016

2017-03-27 Free Webinar: The Latest Updates of Medical Device Regulations in China

2017-02-28 의료기기 중국CFDA등록 설명회 개최

2017-02-28 CIRS will participate in Korea KIMES 2017 international medical instrument equipment exhibition

2017-02-27 The Seminar of Medical Device Regulation and Registration in China

2017-02-22 CIRS is to Attend MEDinISRAEL 2017

2016-08-15 14 mandatory standards will be put into force from 2017.01.01

2016-08-12 웨비나: 중국 의료기기 시장 진출 전략

2016-08-11 Data Requirements for Medical Device Software Registration

2016-08-02 Free Webinar: How to Access the Chinese Medical Device Market（English/Korean）

2016-07-20 CFDA issued the first batch product for Supervision and Random Checking of Medical Device Clinical Trial

2016-07-13 Guideline for Medical Device Certificate Renewal

2016-06-24 Guideline for Medical Device Registration Certificate Alteration

2016-05-05 Key Points of Clinical Trial Protocol Design for Artificial Lens in China

2016-04-26 On-site Inspection Procedure of Medical Device Clinical Trials in China

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Services

CIRS China

Ms Yolanda Yan (Head office)
Tel: +86-571 8720 6559 | Fax: +86-571 87206533
Email: md@cirs-group.com
Mr. Edwin Wen (Beijing office)
Tel: +86-10 63984062 | Fax: +86-10 63984032
Email: md@cirs-group.com

CIRS Europe

Bryan Zhou
Tel: +353 (1)477 3710

Email: md@cirs-group.com

CIRS Korea
Mr. Junho Lee
Tel: +82 2 6347 8801
Email: md@cirs-group.com