监管政策 - China Association for Medical Devices Industry (CAMDI)

监管政策

The Advice on Deepening the Reform of Review and Approval System and Encouraging the Innovation in Drugs and Medical Devices Issued

2017-10-10

Circular of the General Office of the CFDA on Regulating the Classification of Medical Device products

2017-09-30

Practice and Reflection on the examination and approval of Clinical Trials for Innovative Medical Devices

2017-09-07

ANNOUNCEMENT ON SOLICITING PUBLIC COMMENTS ON THE DECISION ON REVISING THE ‘LAW OF THE PEOPLE'S REPUBLIC OF CHINA ON TENDERS AND BIDS’ AND ‘IMPLEMENTING REGULATIONS ON LAW OF THE PEOPLE'S ......

2017-09-01

Letter on Seeking Comments on the Measures for Conditions and Recordation Management of Clinical Trial Facilities of Medical Devices (Exposure Draft)

2017-08-08

Critical Updates of EU Medical Devices Regulations! China Manufacturers Layout Impacted!

2017-08-08

Announcement of CFDA on the Implementation of the Decision of the State Council on Amending the Regulation on the Supervision and Administration of Medical Devices ([2017] No. 78)

2017-06-23

Summary of 2017 Technical Guidelines for Medical Devices

2017-05-25

CFDA released three announcements on seeking public comment on encouraging drug medical device innovation related policy

2017-05-12

Control the medical device technical review quality at system level

2017-05-08

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