Freyr is a Strategic Regulatory partner providing end-to-end Regulatory solutions and services to Innovator pharma companies during their innovator drug development process.
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Freyr acts as a Swiss Authorized Representative(CH-REP) on behalf of foreign medical device manufacturers during registration and compliant market entry of their products as per Swissmedic Regulations.
Freyr provides United Kingdom Responsible Person (UKRP) services to foreign medical device manufacturers in product registration and market entry in the UK and acts as a single point of contact in the Country for liaison with Regulatory Agency.
Freyr provides End-to-End Post Brexit regulatory support for Pharma, Medical Devices, Cosmetics and Food Supplements manufacturers who are willing to market their products in United Kingdom (UK) and EU.
Freyr provides end to end regulatory support for medical device & IVD manufacturers in product registration, notification, classification across the globe.
Freyr SUBMIT Pro is one of the best eCTD software tool which helps Life science companies in various regulatory submissions to global health Authorities.
Freyr provides Global Regulatory Artwork Management Services & Solutions for life sciences Industry, which include Artwork proofreading, Artwork packaging, Artwork Lifecycle management, Artwork Studio Services.
Freyr SPL/SPM is cloud hosted and On-premise software that supports in electronic Pharma registration & listing management, Labeling Management, PI submission in SPL/SPM Format with Automated notification updates.
Freyr label 360 is a Pharmaceutical Labeling Software that Supports End to End Label Management, Label Tracking and Deviation Management for Pharmaceutical Companies across the Globe.
Freyr provides Regulatory Software, Automation and Digital Transformation Solutions to support Global Lifesciences companies.
Freyr provides End-to-End Regulatory Services in Malaysia to the pharmaceuticals, Medical Device, Food Supplements, and Cosmetic Companies to comply with NPRA Regulations.
Contact Freyr for End-to-End regulatory services in Sri Lanka to comply with NMRA regulatory Requirements.
Freyr provides cosmetic regulatory services in Sri Lanka as per NMRA and CESC during cosmetic product registration, classification, Notification, formulation, claims review, CPSR and technical dossier compilation.
Freyr provides food regulatory services in Sri Lanka as per NMRA and FCA during food product registration, classification, formulation, ingredient assessment and technical dossier compilation.
Freyr provides medical device regulatory services in Sri Lanka during medical device registration, classification and licensing as per NMRA regulatory requirements.
Freyr provides pharma/Medicinal product regulatory services in Sri Lanka as per NMRA during Medicinal Product Registration, Market authorization and Dossier Gap analysis.
Freyr provides regulatory services and solutions in Sri Lanka to comply with NMRA to pharma, medical device, cosmetics and food supplement manufacturer companies.
Freyr provides global unified customer support services that ensures smooth onboarding and rapid troubleshooting.
Freyr’s implementation methodology helps life sciences companies in product compliance with various Health Authority Regulations.
Freyr provides Regulatory compliance consulting services and solutions to global life sciences industry.