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CFDA Key Updates GMP/QMS Overview

Illustration of a laptop computer showing Grace Fu Palma speaking during a presentation for a webinar
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  • Create Date December 18, 2017
  • Last Updated January 6, 2022

CFDA Key Updates GMP/QMS Overview

CFDA Regulatory Changes 2017

China medical device/IVD regulations are complex.

During this session Grace will discuss recent developments in manufacturing regulations including new GMPs, self-inspections, foreign inspections and trends in enforcement. These developments can affect all medical device companies, whether your manufacturing facilities are in China or abroad.

After this 90-minute session you will have a practical understanding of the following compliance issues:

  • Implementation of the new GMPs, including the procedural rules for inspections, preparation, communicating with investigators, resolving issues, and potential penalties.
  • Transfer of manufacturing sites and amendment of manufacturing and device licenses.
  • Policies and rules on contract manufacturing for medical devices.
  • Handling self-inspections and evaluations of past compliance, including recent examples.

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