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Freyr Digital

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industries
bio-pharma
medical devices
consumer products
innovation
Regulatory

publishing automation
Regulatory intelligence automation
global registration for MedTech
global medical literature monitoring automation
labeling and artwork

global label content QC automation
artwork generation - automation
global medical literature monitoring automation
scientific document translation automation
content-to-carton
safety

global medical literature monitoring automation
scientific document translation automation
ICSR automation
clinical

scientific document QC automation
scientific document translation automation
bespoke
Freyr.NEXT
approach
products
Regulatory information management

Freyr SPAR
Freyr IDENTITY
labeling management

Freyr LABEL 360
Freyr SPL-SPM
Freyr Artwork 360
Regulatory intelligence

Freyr IMPACT
Freyr GLASS
Freyr iREADY
submission management

Freyr SUBMIT PRO
Freyr rDMS
Freyr SUBMIT Track
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case studies

Accelerated AnnexH Report Generation with RIMS Software
Effective Compliance of Cosmetics Formulae with Freyr iREADY
End-to-End Gap Analysis for IDMP Readiness Across Europe
End-to-End Implementation of A Validated Document Management System (DMS) for Labeling on OpenText™
First-Time-Right Solution For 99.7% Tasks for UDI Submission
Freyr SUBMIT PRO for Compliant eCTD Submissions
Global Product Registration Support to a Japan-based Healthcare Organization
Regulatory Compliant eCTD Submission with Freyr SUBMIT PRO
Successful LCM Submissions and Validation with Freyr SUBMIT PRO
Successful Management of Product Registrations with Freyr SPAR
Successful Submission of 150+ MAs Within 1 Month With 50% Increase in Cost Benefits

Success Stories

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life @ Freyr