Blogs

August 16, 2017

Interpretation to CFDA’s Quality Management of Medical Device Clinical Trials

A. About the one-year validity period of the registration test report of medical device clinical trials Article 7 of the “Medical device clinical trial quality management practices” provides: “quality inspection […]
August 15, 2017

Growth Factors Of The Chinese Medical Device Industry

Major Growth Factors These 4 major growth factors are pushing China’s medical device industry into the world’s 2nd largest: As a sub-industry of the pharmaceutical industry, medical device industry accounted […]
August 14, 2017

Policy Diagram: “Amendments to the Registration Management Measures of in Vitro Diagnostic Reagents”

Understanding to the “Amendments to the Registration Management Measures of in Vitro Diagnostic Reagents” The reason of the amendments: The development of in vitro diagnostic technology, the increase of usage […]
August 14, 2017

Review of the Rapid Growing China’s Cardiovascular Device Market

China med Device, LLC provides market access research for Western medical device companies.  Recently MinSheng Pharma published an in-depth analysis on China CVD market. CVD is not only the top […]
August 11, 2017
innovation

Interpretation to the Relevant Issues about the Fast Approval Track for Innovative Medical Devices

China Food and Drug Administration (CFDA) pays high attention to the innovation and development of medical device industry. In order to better implement the “Fast Review and Approval Track for the […]