Market Potential and Product Approval
Webcode 24062502
Dipl.-Ing. Stefan Fischer
Cisema (Hong Kong) Limited
Founder & Managing Director;
Stefan Fischer is currently managing director
of Cisema (Hong Kong) Ltd. in Hong Kong His areas of expertise are product safety approvals as well as customs regulations in the PRC. This includes
as well as medical technology registrations and "China Compulsory Certification" (CCC).
More information please click here.
BA/LLB, RAC Hamish King
Cisema (Hong Kong) Limited
Director Business Development & Sales
Dipl. BWL Guo Ning
Cisema Beijing Consulting Ltd.
General Manager Beijing
04-05/06/2024
04-05/06/2024
9 - 12 am CET
online
online
Veranstaltung - 1,190 € zzgl. MwSt.
The attendance fee includes the download of documentation and your certificate after taking a short test.
Veranstaltung - 1,190 € zzgl. MwSt.
The attendance fee includes the download of documentation and your certificate after taking a short test.
Verena Planitz
Conference Manager
+49 6221 500-655
v.planitz@forum-institut.de
Would 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.
Medical Device Market in China and Introduction to NMPA Registration (Part 2)
End of day 1
Break
End of seminar
The participants are warmly invited to also contribute their own experiences for a thorough exchange! Please send your topic at least 10 working days before the start of the webcasts to v.planitz@forum-institut.de
Once you have registered for an event, we will send you the access information for your customer portal. Click here to log in to the customer portal using your email address and password. Please ensure you can access the customer portal before the day of the event.
All important or additional information and personal documents are available in your personalised customer portal. This is also where you start your online courses. If you do not have access to the customer portal yet, you can easily register here.
On the day of the event, you kick off your online training in the customer portal by clicking ‘Participate’ directly in the respective event. You will then be redirected to the Learning Space.
Learn more about our online events here.
Seminar content: 100% of the participants’ feedback was very good or good. (June 2022)
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Fachwissen für Informationsbeauftragte!
Very informative on various topics of Medical device registration in China
Expectations: to get an overview of the most important steps / issues in MD registration in China. My expectations were met.
Ms. Anna King: clear speaking and very interesting to listen
