Freyr provides end to end regulatory support for Food/dietary supplements manufacturers in product registration/notification and classification across the globe.
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Freyr SPL/SPM is cloud hosted and On-premise software that supports in electronic product registration; listing management, Labeling Management, PI submission in SPL/SPM Format with Automated notification updates.
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 end to end regulatory support for medical device & IVD manufacturers in product registration, notification, classification across the globe.
Freyr Reports provide Regulatory Intelligence, Market Intelligence, Trend Analysis Reports which include information on global/regional Regulatory guidelines, market trends, forecasts; insights, market analysis, competitive intelligence, opportunity, market potential as per region specific HA’s across the globe.
Freyr provides regulatory services and solutions in Mexico to comply with COFEPRIS for pharma, medical device, cosmetics and food supplement manufacturer companies.
Freyr provides regulatory and product registration support in Nigeria to comply with NAFDAC to pharma, medical device, cosmetics, and food supplement manufacturer companies.
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 services and solutions in Thailand to comply with Thailand FDA for pharma, medical device, cosmetics, and food supplement manufacturer companies
Freyr Artwork 360 is one of the best Artwork Management Software tool which helps Life science companies to simplify the complexity of Artwork Management Process
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.