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We Can Make You Obtain Medical Device Registration Certificates from the Chinese National Medical Products Administration (NMPA)


Our regulatory consultants are diligent in preparing and reviewing medical device registration documents. We will take the following steps to minimize additional documentation requests from the approval body and other delays:


  • Medical device registration in China;

  • Analyze the dynamics of registering your medical device in China market;

  • Coordinate registration testing in lab authorized by China authorities and communicate throughout the testing process;

  • Design clinical trials needed for registration;

  • Prepare and manage product technical requirements and regulatory documentations as required;

  • Translate documents for registration application or filing to Chinese;

  • Address any questions or requests from the China government agency;

  • Obtain approval and send the final registration approval certificate to the client.

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