News & Events

2018-09-18 How to Confirm the Operational Life of Active Medical Devices in China

2018-09-11 Tips on Soft Contact Lens Registration in China

2018-09-11 China Medical Device Authority Restructured as NMPA

2018-08-09 Free Webinar: The Latest Regulatory Updates of Medical Device in China

2018-04-10 Free Webinar The Guideline about Accepting the Medical Device Oversea Clinical Trial Data

2018-04-09 2017 Annual Report for Medical Deivce Registration in China

2018-02-02 CFDA Announcement on Releasing Good Manufacturing Practice for Medical Devices ([2014] No. 64)

2018-02-01 Will the Clinical Trial Condition Differences Affect the CFDA Oversea Clinical Trial Data Acceptance?

2018-01-25 How Will the Subjects Difference Affect the Oversea Clinical Trial Data Acceptance

2018-01-18 Technical Review Differences for The Oversea Clinical Trial Data Acceptance

2018-01-17 CFDA Issued Eight Registration Guidelines

2018-01-16 The Oversea Clinical Trial Data Submission Condition and Acceptance Requirements

2018-01-12 Accept the Medical Device Oversea Clinical Trial Data Technical Guideline

2018-01-11 CFDA Issued Six New Guidelines

2018-01-10 CFDA Clinical Trial Design Guideline

2017-12-26 CFDA Issued Four Registration Guidelines

2017-12-25 CFDA Issued Two Clinical Evaluation of Technical Review Guidelines

2017-12-19 CFDA Suspend The Import of Two Medical Devices in China

2017-12-18 CFDA Issued Ten Registration Guidelines

2017-12-13 CFDA Medical Device Registration Administration Fee Standard (By 12/13/2017)

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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

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Mr. Junho Lee
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Email: md@cirs-group.com