Drug Development Regulatory Services
Regulatory Strategy and Insights
Dossier Authoring
Post Approval/Lifecycle Management
Country-specific Regulatory Services
Global Health Authorities-Specific Services
EU CTR Submissions
Regulatory Publishing and Submissions
Regulatory Labeling Services
Regulatory Artwork Services
Clinical Services
Non-Clinical Services
Regulatory Toxicology Services
Clinical and Non-Clinical Consulting and Strategic Services
Automation in Medical Writing
Literature Monitoring
ICSR Management
Aggregate Reporting
Pharmacovigilance Risk Management
Signal Management
Audit Support and Training Compliance
Quality Assurance and Analysis
Local Safety Representation
Safety Regulatory Intelligence
Database Services & Technology Solutions
Manuscripts and Publications
Promotional and Non-promotional Content Curation
Creative Scientific Design Studio
Promotional Materials Review - MLR
FDA Ad Promo Submissions - OPDP 2253
Content Management
CAS Consulting
SOP Development
GxP Audit
CSV and CSA
QMS Remediation & Establishment
End-to-end Compliance Services
Global Regulatory Intelligence
Device Registration Americas
Device Registration Europe
Device Registration China
Device Registration Japan
Device Registration South Korea
Device Registration Australia
Device Registration: Rest of the World
In-Country Representation
Translation Support
Device Documentation
Labeling Services
Artwork Services
Technical Writing Services
RA Staff Augementation Services
Regulatory Consulting
Clinical Evaluation
Performance Evaluation
Post Market Surveillance
Lifecycle Management
Literature Search Protocol and Review
ISO 13485 Certification
MDSAP
FDA 21 CFR Part 820 Quality System Regulation (QSR)
ISO 14971 Risk Management Consulting
SaMD Registration in the US
SaMD Registration in the EU
Australia TGA Software as Medical Devices (SaMD) Registration
SaMD Registration in South Korea
Human Factors Engineering for Medical Devices
Market Intelligence Service
Formulation and Ingredient Review
Labeling Review
Claims Review
Safety Assessment And Toxicology
Cosmetic Product Information File (PIF)
Go-to-market and Legal Representative (LR)
Cosmetic Testing
Modernization of the Cosmetics Regulation Act of 2022 (MoCRA)
Cosmetic Regulatory Intelligence
EUDR Compliance Services for Cosmetics Industry | Freyr Solutions
Food Product Service
Global Herbal Supplement Compliance Services
Food Product Claims Substantiation
Food Labeling Requirements and Claims Review
Food Product Dossier Compilation
Food Legal Representation
Ecolabeling Regulatory Support
GMPs for Dietary Supplements
Food Regulatory Pathway Reports
Food Product Compliance
Food Ingredient Assessment and Food Formulation Review
Food Supplement Classification
Food Supplement Registration
Alcoholic Beverage Regulatory Compliance
EUDR Compliance Services for Food Industry | Freyr Solutions
Novel Food Registration
NDIN/GRAS (US/US FDA)
US FDA Food Facility Registration
Chemical Data Scouting
Chemical Scientific Assessment Reports and Position Paper Report
Supply Chain Regulatory Compliance
Chemical Packaging Regulations
Biocidal Product Disinfectants - Biocidal Product Regulations
Regulation of Tobacco Products
Chemical Safety Data Sheet
Pet Care Products Registration
General Product Safety Regulation (GPSR)
Global REACH Regulatory Compliance
Chemical Toxicological Risk Assessment
EUDR Compliance Services for Chemical & general consumer product | Freyr Solutions
Sustainability Regulatory Services
EUDR Compliance I Food, Cosmetics & Chemicals
At the heart of Freyr Digital’s suite of Regulatory software prowess lies the knowledge we have gathered over decade. In a world overflowing with data, we navigate with wisdom, carve out new paths with creativity, and drive forward with the most advanced tech solutions. Know More
