Latest NEWS: EP vote on revised EU MDR & IVDR +++ Latest DOCUMENT in our Library: Swiss Medtech guide or how to ensure you can sell-off all your legacy medical devices after 26.05.2024 +++ Manufacturer self-declaration for legacy devices in STORE now +++ WEBINAR on IVDR legacy extension and EUDAMED gradual roll-out +++ Our memberships give access to our comprehensive Library of documents, immediate regulatory alerts,...
Latest NEWS: EP vote on revised EU MDR & IVDR +++ Latest DOCUMENT in our Library: Swiss Medtech guide or how to ensure you can sell-off all your legacy medical devices after 26.05.2024 +++ Manufacturer self-declaration for legacy devices in STORE now +++ WEBINAR on IVDR legacy extension and EUDAMED gradual roll-out +++ Our memberships give access to our comprehensive Library of documents, immediate regulatory alerts,...

We make European MDR and IVDR

Did you know that QMS as per ISO 13485:2016 requires to have a system in place to monitor relevant regulatory requirements and related changes ?
MDlaw offers exactly such system!
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