Would you like to successfully register your medical device or IVD with China’s NMPA? Do you have detailed and specific questions about latest regulations and changes? Then attend our webcasts and learn more about the new Chinese regulation for medical devices, how to perfect your pre-market registration and post-market surveillance: Our local experts will provide you with brand new information.
December 7 – 8, 2021 | 9 – 12am CET | Masterclass in China Registration for Medical Device & IVD
Topics
- Update your regulatory knowledge
- Pre-Market Registration (PMR): Minimalise your efforts and costs
- Acceptance of European registration tests
- Clinical pathways: From feasibility study report to a clinical trial
- Perfect your cooperation with your NMPA legal agent
- Chinese IFU and label
Aims and objectives
China for advanced: Get your deep dive on the latest regulatory changes, optimisation of PMR and Chinese post-market surveillance system.
The two-day webcast will provide detailed updates about recent regulatory changes in China – including the new medical device law Order 739 which came into force on 1st June. Last, but not in least, our local experts will address the PMS and related change management with many examples.
Questions and discussions are explicitly welcome. Take advantage of the interactive opportunity to talk directly to local experts during the Q&A sessions.
Who should attend
The webcasts are aimed at specialists and managers in the medical device and IVD industry who are managing medical device marketing authorisation in China. Good knowledge of the Chinese medical device market and its legal framework is an important prerequisite. This online course is of particular interest for the following departments:
- Regulatory, clinical and quality affairs
- Strategy & corporate development
- Product management
- Distribution and sales
Contact Cisema if you would like to learn more.
