Freyrsolutions

Freyr provides regulatory strategy consulting services for medical device manufacturers looking for global expansion in complex markets like APAC, MENA & LATAM and supports in device registration, classification, assistance with notified body selection and regulatory submissions.

Freyr provides regulatory supports for medical devices and In-vitro diagnostics (IVD) manufacturers in registration, regulatory submissions, dossier compilation, GAP analysis, premarket notification, local agent services and classification as per country-specific regulatory requirements for compliant market entry.

Freyr provides Staff Augmentation Consulting services for medical device manufacturers that span across several Regulatory functionalities from associate to expert level resources and 24X7 time zone coverage model to support multiple time zone and office coverage.

Freyr helps medical device manufacturers with language translation, editing of medical device technical information in IFU, DSURs, SUSARs, Package inserts & labels for submission & approval process as per targeted regional languages with compliance to ISO 17100:2015 & ISO 9001:2008 standards.

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 Information Management solutions for Life Sciences companies that enables end-to-end tracking of Regulatory activities related to various kinds of products like Pharmaceuticals, Biologics and Cosmetics.

Freyr provides Labeling management solutions for Lifesciences companies to comply with global Health Authority regulations.

Freyr provides regulatory intelligence solutions for Lifesciences organizations for compliant market entry of products across the globe.

Freyr offers eCTD publishing, submission and document management solutions for life sciences organizations for compliant product market entry across the globe.

Freyr’s workforce management HRMS software helps companies to achieve visions of business metrics to evaluate the exact number of workforces required for work at a given period.

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.

Freyr label 360 is an end-to-end label management software that helps Pharmaceutical/drug manufacturers in global label compliance

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 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 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 SUBMIT Pro is an eCTD software tool that helps life sciences companies to be compliant with eCTD submissions and publishing.

Freyr rDMS is an end-to-end regulatory document management system software that helps life science organizations in managing regulatory documents for compliance.

KonnectCo is a workforce management HRMS software, that helps companies in managing individuals requirements with company goals.

Freyr provides cloud based technology regulatory product suite for Pharma & Biopharmaceuticals organizations for end-to-end Regulatory Management.

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.