Advocacy Actions

2015-04-14 > Shanghai

Shanghai Intellectual Property Administration Briefing

Shanghai Intellectual Property Administration Briefing

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2015-04-14 > Beijing, Shanghai

Comments on "Requirements to Registration Dossier for Medical Software" submitted to CMDE

The Center of Medical Device Evaluation (CMDE) of the CFDA had issued a Call for Comments on the Requirements to the Registration Dossier for Medical Software. Based on the input from member companies the EUCCC had submitted consolidated comments and suggestions to the CMDE

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2015-04-10 > Shanghai

Seminar on Innovation and IP

Seminar on Innovation and IP

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2015-04-03 > Beijing, Shanghai

Comments to the "Principles for the Scope of Registration Certificates" Submitted to the CMDE

The Center of Medical Device Evaluation (CMDE) of the CFDA has asked for comments on the "Principles of the Scope of Registration Certificates". Based on the input of member companies, the HCE Working Group of the EUCCC in cooperation with COCIR has submitted their comments and recommendations to the CMDE.

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2015-04-02 > Shanghai

Education Roundtable

Education Roundtable

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2015-04-01 > Shanghai

EUCCC Vice Chairman Meeting with SCOFCOM DG Shang Yuying

EUCCC Vice Chairman Meeting with SCOFCOM DG Shang Yuying

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2015-03-26 > Shanghai

Meeting with German Consul on Foreign School’s Operation in Shanghai

Meeting with German Consul on Foreign School’s Operation in Shanghai

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2015-03-26 > All chapters

Meeting with the EU Delegation (DG SANTE) on eHealth Roundtable with NHFPC

The EU Delegation (DG SANTE), COCIR and EUCTP discussed the backgroud, status and actions moving forward, on the eHealth Expert Roundtable, which industry is trying to have with NHFPC

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2015-03-23 > All chapters

Meeting with Department of Medical Device Supervision of the CFDA on actual issues on post-market surveillance

A Meeting of delegates of European and American Company Delegates on Actual Issues related to Post-Market Surveillance

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2015-03-20 > All chapters

CFDA Call for Comments on Issue of Export Certificates for Medical Devices

Comments on the CFDA's Draft of the < Administration Rules for the Issue of Export Certificates for Medical Devices >

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