Regulatory document matrix for medical devicesFor 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.
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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