Overview
Freyr offers a comprehensive range of services for global Regulatory compliance requirements for large, medium and small Medical Device and In Vitro Diagnostic Device (IVD) companies. Freyr’s global team of qualified professionals have expertise in governing the development, performance testing and validation, manufacturing, labeling and registration as well as distribution of Medical Device and In Vitro Diagnostic Devices (IVD) worldwide.
Freyr assists device developers, manufacturers, importers and distributors of Medical Device and In Vitro Diagnostic Device (IVD) worldwide in areas of:
Freyr Expertise and Advantages
Proven Expertise
Freyr is uniquely positioned to deploy best vertical/divisional in-house experts to provide the best Regulatory approach, specifically for companies with portfolio of mixed products. The customized nature of Freyr services is synchronized keeping in mind our customers’ growth strategy and product portfolio.
Freyr offers you a robust combination of technology and Regulatory expertise to ensure product continuity, label compliance, and data quality. We are committed to partnering with companies by providing strategic guidance as they develop, advance and innovate devices.
- 1400+
Global Customers
and Growing - 2300+
Global
Regulatory Experts - 120+
Countries Constitute
our Regional Medical
Device Regulatory Services Portfolio - 325+
Medical Device
Companies Have
Chosen Us as Their
Strategic Partner - 3
Forbes Global Top 5
Medical Device
Companies Have
Chosen Us as Their
Strategic Partner
