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Regulatory Affairs for Medical Devices

Overview

Regulatory Affairs for Medical Devices Overview

Freyr offers a comprehensive range of services for global Regulatory compliance requirements of large, medium, and small medical device and In Vitro Diagnostic (IVD) device companies. Freyr’s global team of qualified professionals has expertise in governing the development, performance testing and validation, manufacturing, labeling, and registration, as well as the distribution of medical devices and In Vitro Diagnostic (IVD) devices worldwide.