Medical Device Market Authorisation for Advanced: Pre-Market Registration and Post-Market Surveillance in China
Webcode 24092500
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
Chief Operating Officer
Dipl. BWL Guo Ning
Cisema Beijing Consulting Ltd.
General Manager Beijing
10-11/09/2024
10-11/09/2024
9 - 12 am CET
online
online
Event - 1,190 € plus tax
The attendance fee includes the download of documentation and your certificate.
Event - 1,190 € plus tax
The attendance fee includes the download of documentation and your certificate.
Verena Planitz
Conference Manager
+49 6221 500-655
v.planitz@forum-institut.de
Interested in establishing a strong presence in the Chinese medical devices market? Join our training to gain valuable insights into the latest Chinese regulations governing medical devices, and discover strategies to optimize your pre-market registration and post-market surveillance. Benefit from the expertise of our local specialists, who will share up-to-date information to enhance your success
Explore advanced insights into China's latest regulatory changes, PMR optimization, and the post-market surveillance system in our seminar.
Stay informed with detailed updates on recent regulatory shifts, notably the 2021 medical device law and its ongoing subsidiary regulations. Our local experts will share practical examples, addressing PMS and change management.
Your questions and discussions are encouraged! Seize the interactive opportunity to converse directly with local experts during Q&A sessions. Join us for a streamlined, informative experience.
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