Freyr with highly skilled professional services team helps life sciences organization in on-premise regulatory software deployment as a part of regulatory system implementation phase.
Facing issue in account approval? email us at info@ipt.pw
FREE SEO TOOLS to Explore
Freyr’s RIMS is a regulatory information management system that helps life sciences companies to manage the detailed product information as per ISO IDMP standards.
Freyr XEVMPD provides Data Management support that includes a comprehensive approach from organization skill assessment, development of implementation roadmap to end-to-end process implementation.
Freyr IDENTITY helps medical device manufacturers to meet FDA mandated UDI regulatory compliance with GxP practice 21 CFR Part 11 regulations.
Freyr IDMP is an Cloud hosted IDMP Software that provides data management solutions for medicinal products/pharmaceutical manufacturers to be compliant with ISO IDMP Standards and EMA requirements.
Freyr provides Regulatory compliance consulting services and solutions to global life sciences industry.
Freyr’s implementation methodology helps life sciences companies in product compliance with various Health Authority Regulations.
Freyr provides global unified customer support services that ensures smooth onboarding and rapid troubleshooting.
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 Label 360 is a Regulatory Labeling Management Software that helps Pharmaceutical Companies in Managing global and regional labeling, CCDS creation and updation, core to local label alignment.
Freyr Label 360 is a Regulatory Labeling Management Software for Pharmaceutical Companies, Request for a Demo to know more.
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 pharma/Medicinal product regulatory services in Sri Lanka as per NMRA during Medicinal Product Registration, Market authorization and Dossier Gap analysis.
Freyr provides medical device regulatory services in Sri Lanka during medical device registration, classification and licensing as per NMRA regulatory requirements.
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 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.
Contact Freyr for End-to-End regulatory services in Sri Lanka to comply with NMRA regulatory Requirements.
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 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 medical device regulatory services in Nigeria during medical device registration, classification, and licensing as per NAFDAC regulatory requirements.