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    Clarvin is exclusively focused on Regulatory Affairs and Quality Assurance for Medical Devices and IVD.
    We support our clients with all questions and aspects regarding RA & QA and offer flexible, full-service solutions.
    Together with our partner companies, Devicia, Limulus Bio, Lea Reg & Kickfile we support you with Strategy, QMS, Regulations, Biocompatibility, Medical Writing and Clinical Investigation, EU authorized representative, UK responsible person.

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    Riddargatan 12B
    114 35 Stockholm
    Sweden
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