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Freyr, as a proven Regulatory partner, provides end-to-end Medical Device Regulatory services that span across decoding Medical Device classification, compiling Device documentation, Medical Writing, Device Registration and acting as an in-country representative. We customize the process with respect to service and software assistance for end-to-end device approvals. With our presence across the continents, Freyr offers Regulatory services for market entry and Regulatory compliance across all regions. Our dedicated team consist of a mixed pool of expertise offering one-stop solution for all the Regulatory needs.
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