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Found 65 results for any of the keywords freyr team. Time 0.010 seconds.

TGA Marketing Authorization Application, MAA submission, TGA Registrat

Freyr provides Regulatory Affairs services in Australia(TGA) for pharmaceutical products manufacturers during Marketing Authorization Application (MAA) Submissions, registration and entry into Australian Register of Ther
https://regulatoryaffairs.freyrsolutions.com/tga-marketing-authorization-application-maa - Details - Similar

CTD Dossier Template, Dossier Template, CTD templates, CTD Format

Freyr provides customized CTD dossier templates during preparing developing applications like MAA, IND, NDA, BLA, ANDA and IMPD in the CTD Format.
https://regulatoryaffairs.freyrsolutions.com/ctd-dossier-templates - Details - Similar

Health Authority Interactions, HA Queries, Pre-submission Meeting, HA

Freyr provides Regulatory Affairs support during the health authority interactions, HA queries, pre-submission meeting, HA requirements, health authority meeting, health authority requirements, pre-submission meeting req
https://regulatoryaffairs.freyrsolutions.com/health-authority-interactions-pre-submission-meetings - Details - Similar

Regulatory Submission Roadmap, Regulatory Intelligence, Regulatory Str

Freyr provides Regulatory Affairs Consulting Services during regulatory submission roadmap, regulatory intelligence, regulatory strategy, regulatory submission requirements and regulatory framework.
https://regulatoryaffairs.freyrsolutions.com/regulatory-submission-road-maps-regulatory-intelligence-services - Details - Similar

Regulatory Strategy Consulting, Regulatory Consulting, Regulatory Affa

Freyr provides Regulatory Affairs support during the regulatory strategy consulting, regulatory consulting, regulatory affairs strategy, regulatory affairs consulting, pharmaceutical regulatory consulting services and re
https://regulatoryaffairs.freyrsolutions.com/regulatory-strategy-consulting-services - Details - Similar

Regulatory Services in Japan, Regulatory Affairs Japan, PMDA Regulatio

Freyr provides End-to-End Regulatory Services in Japan to the pharmaceuticals, Medical Device, Food Supplements, and Cosmetic Companies to comply with PMDA Regulations.
https://japan.freyrsolutions.com/ - Details - Similar

Best eCTD Software Tool for global eCTD Submissions

Freyr SUBMIT Pro is one of the best eCTD software tool which helps Life science companies in various regulatory submissions to global health Authorities.
https://www.ectdtool.com/ - Details - Similar

Structured Product Labeling, SPL Software, SPM Software | Freyr SPL/SP

Freyr SPL/SPM is a cloud hosted and On-premise SPL SPM software that helps pharmaceuticals/drug manufacturers in labeling management submission in SPL/SPM Format for USFDA and Health Canada.
https://www.freyrdigital.com/products/labeling-management/spl-spm - Details - Similar

Testimonials | Freyr Digital

Thank you, team, for your efforts in supporting several key launches over the last few months. Launches play a critical role in the growth of our business. Thank you to the entire team for your efforts and support in mak
https://www.freyrdigital.com/testimonials - Details - Similar

Structured Product Labeling, Structure Product Monograph Software

Freyr SPL/SPM is cloud hosted and On-premise software that supports in electronic drug registration listing management, Labeling Management, PI submission in SPL/SPM Format with Automated notification updates.
https://www.freyrsplspm.com/ - Details - Similar

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