Registration procedure of Medical Devices in China and Japan

The Asian market offers enormous opportunities for manufacturers of Medical Devices - but not without risk. Recognizing and understanding the Asian mentality and the national policies of the Asian market is essential and can make the difference between success and failure.

Content

  • Presentation of regulatory requirements for the approval of Medical Devices in China and Japan
  • Case studies: Registration of Medical Devices
  • Costs structure of the registration procedure
  • Cultural features and first hand reports
Details
Type: 
Inhouse
Target audience: 
This seminar is aimed at specialists and executives of Medical Device manufacturers. Staff from the following departments will benefit from the event: Regulatory Affairs, Quality Management, Product Management, Marketing, Sales.
Language: 
German
Requirements: 
Knowledge of European Medical Device guidelines and EN ISO 13485 is recommended but not necessary.
Fee: 
480 Euro + 19% MwSt. = 571,20 Euro
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