News & Events

2017-06-20 How to Confirm the CFDA Registration Unit for Medical Device Software
2017-06-16 How to Compile Medical Device Software Registration Application Dossiers.
2017-06-13 Preparation of Medical Device Technical Requirements
2017-06-07 Medical Device Software CFDA Registration
2017-06-02 How to Compile Medical Device Software Describing Documents for CFDA Registration (with the sample document created by CIRS)
2017-05-27 Medical Device Software Version Monitoring and Case Study
2017-05-19 No More Clinical Trials for Some Class II and III Medical Devices Registration in CFDA (Updated Version)
2017-05-18 Full Life Circle Management for the New Medical Devices
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
Contact Us
CIRS China

Ms. Shuo Wang (Head office)
Tel: +86-571 8720 6559 | Fax: +86-571 87206533
Mr. Edwin Wen (Beijing office)
Tel: +86-10 63984062 | Fax: +86-10 63984032

CIRS Europe

Ms. Louise Halpin
Tel: +353 41 9806 916 | Fax: +353 41 9806 999


CIRS Keroa
Mr. Junho Lee 
Tel: +82 2 6347 8801