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Freyr is a leading, niche, full-service global Regulatory Solutions and Services Company supporting, Large, Medium and Small size global Life sciences companies, (Pharmaceutical | Generics | Medical Device | Biotechnology | Biosimilar | Consumer Healthcare | Cosmetics | Chemicals) in their entire Regulatory value-chain; ranging from Regulatory Strategy, Intelligence, Dossiers, Submissions etc. to Post- Approval / Legacy Product Maintenance, Labeling, Artwork Change Management and other related functions.
Freyr offers complete suite of Regulatory tools and software services that match client requirements; be it publishing and submissions, labeling, Regulatory intelligence, Regulatory document management, trial master files, IDMP, and end-to-end Unique Device Identification (UDI) compliance solution. Freyr’s proprietary Regulatory tools are flexible, intuitive, user-friendly, ready-to-use, efficient, secured and cloud-hosted, which enables organizations to streamline all their Regulatory activities.
Freyr is a trusted partner, providing end-to-end Regulatory services across 8 of the Forbes* Global Top 10 Healthcare / Life Sciences, Mid-market $1+ Billion Bio Pharma, and Several Small-Medium, Fast Growing Life Sciences companies, CROs and Standards agencies.
Freyr is one of the few global companies to have pioneered specialized Centers of Excellence (CoEs) exclusively focusing on the entire Regulatory value-chain which are supported by rapidly growing global teams of 1000+ Regulatory Professionals.
Freyr is a leading, niche, full-service global Regulatory Solutions and Services Company supporting, Large, Medium and Small size global Life sciences companies, (Pharmaceutical | Generics | Medical Device | Biotechnology | Biosimilar | Consumer Healthcare | Cosmetics | Chemicals) in their entire Regulatory value-chain; ranging from Regulatory Strategy, Intelligence, Dossiers, Submissions etc. to Post- Approval / Legacy Product Maintenance, Labeling, Artwork Change Management and other related functions.
Freyr offers complete suite of Regulatory tools and software services that match client requirements; be it publishing and submissions, labeling, Regulatory intelligence, Regulatory document management, trial master files, IDMP, and end-to-end Unique Device Identification (UDI) compliance solution. Freyr’s proprietary Regulatory tools are flexible, intuitive, user-friendly, ready-to-use, efficient, secured and cloud-hosted, which enables organizations to streamline all their Regulatory activities.
Freyr is a trusted partner, providing end-to-end Regulatory services across 8 of the Forbes* Global Top 10 Healthcare / Life Sciences, Mid-market $1+ Billion Bio Pharma, and Several Small-Medium, Fast Growing Life Sciences companies, CROs and Standards agencies.
Freyr is one of the few global companies to have pioneered specialized Centers of Excellence (CoEs) exclusively focusing on the entire Regulatory value-chain which are supported by rapidly growing global teams of 1000+ Regulatory Professionals.
Our locations:
United States Of America 150 College Road West, Ste 102, Princeton NJ - 08540 Fax: +1 866 486 6883 Phone: +1 908 483 7958 / +1 908 409 5626
United Kingdom 1 Bell Street, Maidenhead, Berkshire, SL6 1BU Phone: +44 2037 0123 79
India Level 4, Building No. H-08, Phoenix SEZ, HITEC City 2, Gachibowli, Hyderabad – 500081 Phone: +91 40 4848 0999
Freyr provides Regulatory Software Solutions to support Global Lifesciences companies that include Pharmaceuticals, Medical devices, Cosmetics and Food Supplement companies to be complaint.
Freyr Technology