Medical Devices in China - Market Potential and Product Approval in China - Webinar von FORUM Institut für Management GmbH

- Market potential for European companies in the Chinese market - Product approval - National Medical Products Administration (NMPA): Documents, procedures, fees - tips and tricks - Clinical pathways - Post-market Surveillance & Quality Management System - Latest Regulatory Changes and TrendsWould you like to successfully approve and market your medical devices in China as well? Then attend our webcasts and learn more about market potential and product approvals. Our local experts will provide you with comprehensive information - especially on the subject of approval and risks that exist for European medical device manufacturers or importers.

The National Medical Products Administration (NMPA) has been established in China since 2018, replacing the former State Food and Drug Administration (CFDA). The NMPA is responsible for regulating medical devices in China and ensures that the quality and safety of medical devices are standardized. - China is the second largest healthcare market in the world. For many medical device manufacturers, it is a challenge to fulfill the dynamically changing regulatory requirements.It requires knowledge and support to navigate the market successfully. However, China’s large and ageing population makes it an attractive healthcare market that offers numerous opportunities for foreign companies. - If you are looking to enter the Chinese market or seeking deeper understanding to unlock key pain points, our local Hong Kong and China mainland experts can answer all your regulatory questions and help you navigate the market successfully. These two interactive live online trainings will highlight the opportunities and potential of European medical devices and technology for the Chinese market. The requirements for the registration and ongoing compliance of medical devices are described in detail.

This course is aimed at specialists and managers in the medical device and IVD industry who are planning medical device marketing or renewing an existing marketing authorization in China. This online training is of particular interest for the following departments: - Regulatory, clinical and quality affairs - Strategy & corporate development - Marketing and product management - Distribution and sales