Requalite provides Regulatory, quality, and Clinical Study services for in vitro diagnostic and medical device compliance in EU. 
Requalite is located at the heart of Europe, in Munich-Germany. We provide full CRO services for clinical studies as per IVDR/MDR. In addition, we provide Technical and medical writing services to manufacturers of Medical Device and In vitro Diagnostic devices to obtain CE-marking as per EU regulations of MDR (2017/745) and IVDR (2017/746) for entering European market.

Requalite GmbH

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Requalite GmbH

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