Freyrsolutions

Freyr Food Regulatory Affairs provides end to end regulatory support for Food/dietary supplements manufacturers in product notification, classification, and registration across the globe.

Freyr provides end to end Cosmetic Regulatory Services like formulation & ingredient review, label review, claims review, safety assessment & toxicology services, dossier compilation and market entry support.

Freyr provides cosmetic regulatory services in Malaysia that span across cosmetic product registration, classification, Notification, formulation, claims review, CPSR and technical dossier compilation as per NPRA regulation.

Freyr provides food regulatory services in Malaysia that span across food product registration, classification, formulation, ingredient assessment, technical dossier compilation and submission as per NPRA regulations.

Freyr provides medical device regulatory services in Malaysia that span across medical device registration, medical device classification and market entry as per NPRA regulatory requirements.

Freyr provides pharma/Medicinal product regulatory services in Malaysia as per NPRA regulations during Medicinal Product Registration, classification, Market authorization, Dossier Gap analysis and compliant with ACTD.

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 Swiss Authorized Representative (CH-REP) services to foreign medical device manufacturers for their product registration and market entry in Switzerland and acts as a single point of contact in the Country for liaison with Regulatory Agency.

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 Regulatory Software, Automation and Digital Transformation Solutions to support Global Lifesciences companies.

Freyr provides regulatory services and solutions in Mexico to comply with COFEPRIS for pharma, medical device, cosmetics and food supplement manufacturer companies.

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.