Author: freyrsolutions

Freyr Provide the SPL/SPM Software support across entire value-chain with presence in multiple locations like US, Canada, UK, etc. Freyr Provide the SPL/SPM Software support across entire value-chain with presence in... Read More

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 Demo for Freyr SPL/SMM software offered... Read More

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. Request a quote for Freyr... Read More

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 SPL/SPM... Read More

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... Read More

Freyr SPL/SPM tool is an easy to use SPL/SPM Software that manages SPL/Pharma listing lifecycle & validates the output as per USFDA regulations with seamless SPL Submissions. Freyr SPL/SPM tool is... Read More

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. Freyr SPL/SPM is... Read More

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... Read More

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... Read More

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... Read More