Centered on hot fields and hot issues of medical devices, it discusses relevant issues from different perspectives and puts forward topics and proposals to provide a guidance for clinical application, industry regulation and business development.

Particularly introduce the development trend and specific technology of medical devices in clinical application;

Introduce clinical new technology and achievements and bridge the clinical trials and industry;

Report the purchase, measurement, QC and maintenance experience and technology of medical devices

Make deep interview at famous enterprises, experts and celebrities in medical industry from unique perspective;

Analyze the development trend of certain product category and help enterprises to keep a track of market (requiring cooperation with Medical Device Division of China Chamber of Commerce of Medicines & Health Products Importers & Exporters)

Make an insight into the critical regulation documents and policies issued within the industry and provide service for the whole industry;

Report new regulations, procedures and precautions of registration review and provide service for corporate declaration (requiring for cooperation with CFDA Center for Medical Devices Evaluation).

Report product standard development and exchange examination technology;

Introduce specific design and development achievements of products and technology and technical development trend;

Centered on the implementation of Medical Devices GMP, comprehensively report the problems found during implementation, explore solutions and provide service for enterprises;

Centered on life circle maintenance of medical devices, provide management mode and method for manufacture, sales, use and storage of medical devices;

Focus on foreign regulations, policies and advanced management techniques and development trend of medical devices (possible cooperation with China Center for Pharmaceutical International Exchange);

Summarize influential events of medical devices industry occurred in a certain period and proved brief comments;

Immediately publish overseas monitor condition of medical devices AEs (Cooperation with National Center for ADR Monitoring, CFDA).