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We help Medical Device and In Vitro Device companies in Europe with new Medical Device Regulations(MDR) and new In Vitro Device Regulation(IVDR), helps in devel...

Freyr assists medical device manufacturers with 510k submission (510k premarket notification) support which include 510k compilation, E-submission to FDA, queri...

Freyr has extensive global expertise in Quality Management System (QMS) Compliance Services to support medical device manufacturers in establishing quality syst...

Freyr helps the foreign medical device manufacturers in support for registration, Pre-Certification, Post Approval, MAH services, Interaction in local language ...

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