Freyr provides medical device regulatory services in Sri Lanka during medical device registration, classification and licensing as per NMRA regulatory requirements.
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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 regulatory services and solutions in Sri Lanka to comply with NMRA to pharma, medical device, cosmetics and food supplement manufacturer companies.
Freyr provides global unified customer support services that ensures smooth onboarding and rapid troubleshooting.
Freyr’s implementation methodology helps life sciences companies in product compliance with various Health Authority Regulations.
Freyr provides Regulatory compliance consulting services and solutions to global life sciences industry.
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 IDENTITY helps medical device manufacturers to meet FDA mandated UDI regulatory compliance with GxP practice 21 CFR Part 11 regulations.
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’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 with highly skilled professional services team helps life sciences organization in on-premise regulatory software deployment as a part of regulatory system implementation phase.
Freyr provides cloud based technology regulatory product suite for Pharma & Biopharmaceuticals organizations for end-to-end Regulatory Management.
KonnectCo is a workforce management HRMS software, that helps companies in managing individuals requirements with company goals.
Freyr rDMS is an end-to-end regulatory document management system software that helps life science organizations in managing regulatory documents for compliance.
Freyr SUBMIT Pro is an eCTD software tool that helps life sciences companies to be compliant with eCTD submissions and publishing.
Freyr iREADY is a technology based Cosmetic Ingredient Database platform that helps Cosmetic manufacturers in cosmetics ingredients and management of product formulae in global markets.
Freyr IMPACT is a Cloud-hosted Regulatory Intelligence software that offers regulatory Intelligence tracking support & Regulatory intelligence portal that effectively monitors, collects & updates information by analyzing current HA regulations.
Freyr SPL/SPM is a cloud hosted and On-premise software that helps pharmaceuticals/drug manufacturers in labeling management & submission in SPL/SPM Format for USFDA and Health Canada.
Freyr label 360 is an end-to-end label management software that helps Pharmaceutical/drug manufacturers in global label compliance
Freyr SPAR is an on-premise and cloud-hosted Product Registration and Regulatory Information Management System (RIMS) software that helps Life Science organizations to oversee the detailed product information as per ISO standards.