Freyrsolutions

Freyr Artwork 360 is an easy-to-use Artwork PLM Tool that manages Artwork Workflow Management, Artwork Version Tracking, Artwork Proofing & Review, Artwork Digital Asset Library, Artwork Reports and Collaboration Between Stakeholders ect..

Freyr iREADY is a technology based Cosmetic Ingredient Database platform and it provides Regulatory compliance support to manufacturers for cosmetics ingredients and management of product formulae in global markets

Freyr Submit PRO’s in-built eCTD Viewer’s design enables the users to review the Regulatory submissions prepared in the eCTD format standard used by the Lifesciences industry and various Regulatory authorities.

Freyr SPL-SPM Software is an cost-effective solution for your SPL-SPM submissions which has Automated Process for new SPL-SPM submissions and revisions, adheres with 21 CFR Part 11 HL7 standards.

Freyr Label 360 is a Drug labeling software for pharmaceutical Industry and it is a one stop solution for all regulatory labeling needs.

Freyr provides scientific document translation Automation for Lifesciences organizations to solve scientific document Translation challenges.

Freyr provides regulatory support in Supply chain regulatory compliance, Formulation review, Raw material compliance and Document management services in different levels of consumer product development.

Freyr provides End to End Chemical Safety Regulatory Affairs (CSRA) services to consumer products manufacturers in product registration, classification, toxicology assessment, safety data sheet development and regulatory intelligence services as per region specific regulatory requirements for market approvals.

Freyr provides End to End Chemical Regulatory Compliance services to health care consumers like product registration, notification, Formulation review and We offer EU REACH and CLP Registration/Dossier Update, Hazard Communication for quick market access.

Freyr Cosmetics Regulatory Team helps in the cosmetic artwork design with label review, artwork creation and artwork solutions as per the health authority amendments and regulations

Freyr provides end to end Cosmetic Regulatory consultation support, starting from Regulatory intelligence to responsible person services for cosmetics and personal care companies across the globe.

Freyr provides end to end Cosmetic Regulatory Services like formulation, ingredient review, Cosmetic Labeling, Cosmetic Claims, safety assessment, toxicology services, dossier compilation and market entry support.

Contact Freyr for Global End-to-end Food Supplement regulatory services to comply with Health Authority Requirements.

Freyr provides End to end regulatory support for food supplements manufacturers which include registration, classification and process clearances to comply with region-specific regulatory requirements for successful market entry of products across the globe.

Freyr provides end to end regulatory support for Food/dietary supplements manufacturers in product registration/notification and classification across the globe.

Freyr provides Swiss Authorized Representative(CH-REP) services for medical device manufacturers outside the Switzerland as per Swissmedic regulations.

Freyr provides United Kingdom Responsible Person(UKRP) services for medical device manufacturers outside the UK as per MHRA regulations.

Freyr provides regulatory support to the medical device manufacturers in De-Novo registration of medical devices in the USA that span across classification, Pre-Submission/Q-Submission meeting request, risk benefit determination, De-Novo submission package compilation, publishing and creation for Pre-Submissions.

Freyr provides Swiss Authorized Representative(CH-REP) services for foreign medical device manufacturers and acts as Swiss distributor/importer of devices across Switzerland.

Freyr provides Swiss Authorized Representative(CH-REP) services for medical devices and IVD manufacturers in CE marking and labeling support as per Swissmedic regulations.