Regulatory Affairs Consulting, Regulatory Affairs Services, Consultants

Freyrcorp28 Mar, 2024Business

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 the Freyr offices located across the continents, Freyr offers regulatory services for Market Entry and regulatory compliance across all regions. The resources consist of a mixed pool of expertise offering one stop solution for all the regulatory needs.