Freyrsolutions

Freyr Artwork 360 is an Artwork PLM Tool and a one-stop solution to all your Artwork lifecycle management needs. Freyr Artwork 360 is an Artwork PLM Tool and a one-stop solution to all your Artwork lifecycle management needs. Freyr Artwork 360 is an Artwork PLM Tool and a one-stop solution to all your Artwork lifecycle management needs. Freyr Artwork 360 is an Artwork PLM Tool and a one-stop solution to all your Artwork lifecycle management needs. Freyr Artwork 360 is an Artwork PLM Tool and a one-stop solution to all your Artwork lifecycle management needs. Freyr Artwork 360 is an Artwork PL

Freyr iREADY is a technology based cosmetics ingredients database platform that enables manufacturers in management of cosmetics ingredients and product formulae in global markets. Freyr iREADY is a technology based cosmetics ingredients database platform that enables manufacturers in management of cosmetics ingredients and product formulae in global markets. Freyr iREADY is a technology based cosmetics ingredients database platform that enables manufacturers in management of cosmetics ingredients and product formulae in global markets. Freyr iREADY is a technology based cosmetics ingredients

Freyr Submit PRO, an eCTD publishing software that allows the user to track, modify and review of eCTD documents until submissions to Health Authorities. Freyr Submit PRO, an eCTD publishing software that allows the user to track, modify and review of eCTD documents until submissions to Health Authorities. Freyr Submit PRO, an eCTD publishing software that allows the user to track, modify and review of eCTD documents until submissions to Health Authorities. Freyr Submit PRO, an eCTD publishing software that allows the user to track, modify and review of eCTD documents until submissions to Hea

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

Freyr provides regulatory services and solutions in India to comply with CDSCO regulations for pharmaceuticals, medical devices, cosmetics, and food supplements manufacturing companies.

Freyr provides US FDA Medical device registration services for device manufacturers that span across preparation & compilation of necessary documents for 510(k) submissions and successful FDA medical device establishment registration.

Freyr provides FDA De-Novo Submission Services for medical device manufacturers that span across understanding De-Novo classification request and guiding throughout the classification process to obtain FDA clearance for novel devices.

Freyr provides US FDA 510(k) submission services for medical device manufacturers that span across preparation & compilation of necessary documents as per FDA 510(k) submission requirements/regulations.

Freyr assists medical device manufacturers in FDA 510(k) clearance process that includes different types of 510(k) application submissions and preparation of necessary documents to meet USFDA regulatory requirements.

Freyr provides USFDA 510(k) Consultant support for medical device manufacturers that span across 510(k) document preparation & customized solutions throughout 510(k) clearance process for compliant 510(k) submissions as per FDA regulations.

Freyr provides FDA Q-Submission consulting services for medical device manufacturers that span across pre-submission meeting, Post Q-Sub activities, and compilation of device documents as per USFDA regulations.

Freyr provides USFDA Medical device premarket approval process support for class III medical device manufacturers that span across preparation & review of the PMA application for successful PMA submissions as per US FDA regulations.

Freyr provides FDA 513(g) submission support for medical device manufacturers which includes US FDA medical device classification, preparation & review of 513(g) application to comply with CDRH, FDA regulations.

Freyr Provides Medical device regulatory consulting services for device manufacturers that include product registration and market entry in compliance with HA requirements across the globe.

Freyr provides food regulatory services in Malaysia that span across food product registration, classification, formulation, ingredient assessment, technical dossier compilation and submission as per NPRA regulations

Freyr provides medical device regulatory services in Malaysia that span across medical device registration, medical device classification and market entry as per NPRA regulatory requirements

Freyr provides End-to-End Regulatory Services in Malaysia to the pharmaceuticals, Medical Device, Food Supplements, and Cosmetic Companies to comply with NPRA Regulations

Freyr provides pharma/Medicinal product regulatory services in Malaysia as per NPRA regulations during Medicinal Product Registration, classification, Market authorization, Dossier Gap analysis and compliant with ACTD

Freyr provides cosmetic regulatory services in Brazil as per ANIVSA during cosmetic product registration, classification, Notification, formulation, claims review, CPSR and technical dossier compilation

Freyr provides food regulatory services in Brazil as per ANIVSA and CTCAF during food product registration, food classification, formulation, ingredient assessment, technical dossier compilation and submission