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

监管政策

Center for Medical Device Evaluation Actively Promotes the Implementation of Clinical Evaluations of IMDRF Medical Devices

2018-07-16

Notice of the General Office of the State Council on Adjusting the Personnel of the Leading Group of the State Council on Deepening the Medical and Health Care System Reform

2018-07-13

Opinions of the General Office of the State Council on Promoting the Development of “Internet + Health Care”

2018-05-02

Circular of China Drug Administration on Issuing the Guidelines for Review of 4 Registered Technologies Including Insuffiater (2018 No. 15)

2018-04-23

Notification in Issuing Management Catalog for Large Medical Device Deployment Permit (2018)

2018-04-10

Announcement of CFDA on Technical Review Guideline for Registration of Rigid Optics Endoscope (Invasive)

2018-03-29

China Officially Announces the Implementation of Two-invoice System for High-value Consumables

2018-03-22

Circular of the General Office of the CFDA on the implementation of the measures for Supervision and Administration of Online sale of Medical Devices

2018-02-28

CFDA printed and issued the Management Practices for the Revision of the Standard System of Medical Devices

2017-12-26

Announcement and interpretation on the Issuance of the basic requirements on clinical evaluation data for IVD Reagents for the exempted clinical trials (Trial)

2017-11-09

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