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    For the EU and Swiss market

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Regulatory document matrix for medical devices

For the EU and Swiss market

100 CHF plus VAT

  • Download of document matrix for immediate use.
  • MDR und MedDO requirements and references to the relevant articles.
  • Understanding through description of each relevant regulatory document.
  • Highlighting of Switzerland specific requirements.
  • Basis for comparing the required documents based on risk class of device.
  • Customizable in Microsoft Word or Apple Pages format.
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Description

This matrix of relevant regulatory documents for medical devices is useful for manufacturers, EC-REPs, CH-REPs and importers in the EU and Switzerland. It helps to understand and identify at a glance the necessary documents for access to the EU and Swiss markets.

Language

German and English

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