Medical Devices CE Marking

BSI's Medical Devices CE Marking” three day course is designed to provide participants with the knowledge to assist their companies in getting products to market more quickly.

Management personnel responsible for all aspects of CE marking medical devices as well as internal and external auditors will benefit from this course. Participants will gain knowledge of the requirements of the Medical Device Directive and the CE Marking approach. Participants will be able to provide leadership for their organizations when placing medical devices on the market in the European Union


Participants should have experience with or basic knowledge of quality management systems for the medical device industry or experience of the manufacture, design, marketing or use of medical devices.

  • Benefit from CE Marking expertise within your organization
  • Work without uncertainty when placing products on the EU market 
  • Gain recognition as a producer of products with CE Marking
  • Improve the quality and safety of your medical devices

Increase EU market access and boost customer confidence

What is included

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