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MedQdoc Knowledge Hub for eQMS Tools, News and Downloads


Whether you are aiming for ISO 13485 certification and/or to ensure QSR, ISO 14971, MDR/IVDR compliance to get your medical device CE-marked or successfully registered to any other market, these materials are designed to help you.

This knowledge hub includes information on the documentation templates available via MedQdoc, as well as case studies and blog posts to provide you with further inspiration and support on your medical device compliance journey.

Tools and Downloads

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Request a no-obligation MedQdoc demonstration with one of our regulatory compliance specialists to find out how MedQdoc could deliver value to your business.

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Read the latest articles by our quality and regulatory specialists, for a more in-depth look at different aspects of medical device industry regulatory compliance.

Medical Device Blogs

Swedish MedTech Regulatory Summit Presentation

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Medical Device Blogs

Can an eQMS help you with 21 CFR Part 11 Compliance?

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Medical Device eQMS

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