Freyr provides end-to-end Regulatory Affairs services to the Biologics/Biosimilar product companies during BLA submission process, starting from pre-BLA/BPD meetings to further Life Cycle Management (LCM) of the various biological products.
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Freyr is a Strategic Regulatory partner providing end-to-end Regulatory solutions and services to Innovator pharma companies during their innovator drug development process.
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 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.
Freyr provides Regulatory solutions and services for Generic pharma manufacturers to comply with Health Authority amendments and requirements during generic medicine dossier submissions.
Contact Freyr for Nigeria End-to-End regulatory services to comply with NAFDAC regulatory Requirements for Drugs, Medical Devices, Cosmetics, Food Supplement Product registrations.
Freyr provides cosmetic regulatory services in Nigeria as per NAFDAC during cosmetic product registration, classification, Notification, formulation, clams review, CPSR and technical dossier compilation.
Freyr provides food supplements regulatory services in Nigeria as per NAFDAC during food product registration, classification, formulation, ingredient assessment and technical dossier compilation.
Freyr provides medical device regulatory services in Nigeria during medical device registration, classification, and licensing as per NAFDAC regulatory requirements.
Freyr provides pharma/Drug product regulatory support in Nigeria to comply with LFN, NAFDAC during Drug Product Registration, Market authorization, Dossier Gap analysis and Product Approval Meetings.
Freyr provides regulatory and product registration support in Nigeria to comply with NAFDAC to pharma, medical device, cosmetics, and food supplement manufacturer companies.
Freyr provides global regulatory services for Ultrasound machine span across registration, notification and classification in adherence with the regional compliance standards and fast track approvals for Covid-19 emergencies.
Freyr’s regulatory services in India for Ultrasound Machines span across registration, notification and classification as per CDSCO regulations to meet market entry requirements and fast track approvals for Covid-19 emergencies.
Freyr’s regulatory services in USA for Ultrasound Machines span across registration, notification and classification as per US FDA regulations to meet market entry requirements and fast track approvals for Covid-19 emergencies.
Freyr provides global regulatory services for Diagnostic kits span across registration, notification and classification in adherence with the regional compliance standards and fast track approvals for Covid-19 emergencies.
Freyr’s regulatory services in India for Diagnostic Kits span across registration, notification and classification as per CDSCO regulations to meet market entry requirements and fast track approvals for Covid-19 emergencies.
Freyr’s regulatory services in USA for Diagnostic Kits span across registration, notification and classification as per US FDA regulations to meet market entry requirements and fast track approvals for Covid-19 emergencies.
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.