Freyr provides Regulatory solutions and services for Generic pharma manufacturers to comply with Health Authority amendments and requirements during generic medicine dossier submissions.
Freyr provides regulatory services and solutions in India to comply with CDSCO regulations for pharmaceuticals, medical devices, cosmetics, and food supplements manufacturing companies.
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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 services and solutions in Sri Lanka to comply with NMRA to pharma, medical device, cosmetics and food supplement manufacturer companies
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 Solutions to support Global Lifesciences companies that include Pharmaceuticals, Medical devices, Cosmetics and Food Supplement companies to be complaint.
Freyr provides Regulatory solutions and services for Generic pharma manufacturers to comply with Health Authority amendments and requirements during generic medicine dossier submis...
Freyr provides regulatory services and solutions in India to comply with CDSCO regulations for pharmaceuticals, medical devices, cosmetics, and food supplements manufacturing compa...
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 poi...
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 Unite...
Freyr provides end to end regulatory support for medical device & IVD manufacturers in product registration, notification, classification across the globe.
