Freyr provides US agent representation services for medical device manufacturers and serves as a liaison between manufacturing company and FDA to be compliant.
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Freyr acts as a European Authorised Representative (EAR/EC REP) for foreign medical device manufacturers in Europe to ensure their products are compliant with the European Directives and acts as a single Point of Contact in the Country for Liaison with Regulatory Agency.
Freyr provides post-Brexit regulatory scenarios for life Sciences manufacturers in UK & EU to be inline with new regulatory changes.
Freyr provides Brexit regulatory services for life science companies in most Affected areas like Artwork/Labelling/Packaging, Clinical Trials, GMP, MRP/DCP National/Central Procedure, Pharmacovigilance and Trade Barriers.
Freyr provides Global End-to-End post-Brexit regulatory services for Life sciences companies which include Pharmaceuticals, Medical devices, Cosmetics and Food supplements for compliant product market entry.
Freyr provides End-to-end post-Brexit regulatory services in European Union for Life sciences companies which include Pharmaceuticals, Medical devices, Cosmetics and Food supplements for compliant product market entry.
Freyr provides End-to-end post-Brexit regulatory services in United Kingdom for Life sciences companies which include Pharmaceuticals, Medical devices, Cosmetics and Food supplements for compliant product market entry.
Freyr SUBMIT Pro is an cloud hosted, on-premise cost effective eCTD submission software with features like eCTD Submission tracker, Viewer, Validation and rDMS Integration.
Freyr SUBMIT Pro is one of the best eCTD Submission software that suits all kinds of Regulatory eCTD publishing and submission requirements across the globe.
Freyr SUBMIT Pro is an prominent eCTD publishing Software with various features like Inbuilt eCTD validator and viewer, submission tracking, HA query management, rDMS integration and many more.
Freyr provides United Kingdom Responsible Person (UKRP) services to foreign medical device manufacturers in product registration and market entry in the UK and acts as a single point of contact in the Country for liaison with Regulatory Agency.
Freyr provides End-to-End Post Brexit regulatory support for Pharma, Medical Devices, Cosmetics and Food Supplements manufacturers who are willing to market their products in United Kingdom (UK) and EU.
Freyr provides end to end regulatory support for medical device & IVD manufacturers in product registration, notification, classification across the globe.
Freyr SUBMIT Pro is one of the best eCTD software tool which helps Life science companies in various regulatory submissions to global health Authorities.
Freyr Provide the SPL/SPM Software support across entire value-chain with presence in multiple locations like US, Canada, UK, etc.
Request a Demo for Freyr SPL/SMM software offered in cloud Hosted and on-premise deployment model, which suits all SPL & SPM submission requirements.
Request a quote for Freyr SPL/SMM Software, which adheres with 21 CFR Part 11 standards for seamless SPL/SPM submissions to comply with USFDA and Health Canada.
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 SPM is provides a complete solution for the Health Canada SPM requirements and supports in XML product monograph submissions like NDS, ANDSs, SANDSs, SNDS and all subsequent SPM submissions.
Freyr SPL/SPM is cloud hosted and On-premise software that supports in electronic Pharma registration & listing management, Labeling Management, PI submission in SPL/SPM Format with Automated notification updates.