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
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
Risk Management Pharmacovigilance
Signal Management
Audit Support and Training Compliance
Quality Assurance and Analysis
Qualified Person for Pharmacovigilance
Safety Regulatory Intelligence
Database Services & Technology Solutions
Medical Copywriting Services
Medical and Scientific Writing Services
Manuscripts and Publications
Creative Scientific Design Studio
Promotional Materials MLR Review
Medical and Scientific Content Management
FDA Ad Promo Submissions - OPDP 2253
CAS Consulting Services in Pharma
SOP Writing and SOP Review Services
Pharma GxP Audit Services
Pharma CSV and CSA Services
QMS Remediation and Establishment Services
End-to-end Regulatory Compliance Services
Regulatory Artwork Services
Artwork Graphic Studio
Artwork Proofreading
Global Artwork Translation
Artwork Process Consultancy
Printed Packaging Print-Proof Quality Check
e-Leaflet and e-Label
Content to Carton
Artwork Lifecycle Coordination
Global Regulatory Intelligence
Regulatory Strategy Consultation for SaMD
Quality Management Systems Implementation
SaMD Registration in the US
SaMD Registration in the EU
Global Market Expansion for SaMD
SaMD Bespoke Regulatory Solutions
Device Registration Americas
Device Registration Europe
Device Registration China
Device Registration Japan
Device Registration South Korea
Device Registration Australia
Device Registration UK
Device Registration Switzerland
Device Registration: Rest of the World
In-Country Representation
Product Complaints Management
Device Recall, Corrections and Removals
PMSP, PMSR, PMCF, PSUR, Annual Maintenance
Health Hazard Evaluation
Medical Device Translation Services
CE Marking
EU MDR
EU IVDR
European Authorized Representative
Clinical and Performance Evaluation
QMS Consultancy Services
ISO 14971 Risk Management Consulting
QMS Remediation
Compliance & Audit Support
QMS Toolkit
Document Management
Corrective and Preventive Action (CAPA) Management Services
Supplier Evaluation
Regulatory Artwork
Device Documentation
Labeling Services
Technical Writing Services
RA Staff Augementation Services
Regulatory Consulting
Human Factors Engineering for Medical Devices
Market Intelligence Service
Medical and Scientific Communication
Global Regulatory Compliance and Consulting (GRCC)
Formulation and Ingredient Review
Labeling Review
Claims Review
Safety Assessment And Toxicology
Cosmetic Product Information File (PIF)
Go-to-market and Legal Representative (LR)
Comprehensive Artwork Services for Cosmetics
Cosmetovigilance services
Cosmetic Testing
Modernization of the Cosmetics Regulation Act of 2022 (MoCRA)
Cosmetic Regulatory Intelligence
EUDR Compliance Services for Cosmetics Industry
Food & Food Supplements Product Services
Food and Food Supplements Artwork Services
Novel Food Support (NDIN, GRAS, NSF)
Raw Material Specification Compliance
Ingredients/Formulation Compliance
Claims Review, Substantiation, and Notification Support
Food and Food Supplement Classification: A Global Overview
Manufacturing Facility Registration Support (FFR/FBO/Site license)
Labeling Compliance
Dossier Compilation Support
Food Product Registration Service/Notification
Legal Representation (LR) Support
Regulatory Audit and Training Support (GMPs, GHP, HACCP)
Food Regulatory Pathway Reports
Categories Supported
Herbal Supplements (Botanical Extracts)
Medical Foods / FSMP
Organic Foods
Probiotics, Prebiotics, Postbiotics & Synbiotics
Processed Food Products
Alcoholic Beverages
Sustainability Services
Recycling Logo Content and Design Support for Food and Food Supplements
Navigate EPR, PCR, PPWR & SUP Compliance with Confidence!
EU Deforestation Regulation Services
Ecolabelling Regulatory Support
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
Ecolabeling Regulatory Support
Chemical Safety Data Sheet
Household and Chemical Products Artwork Services
Sustainability Consulting Services
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
EUDR Compliance | Food, Cosmetics & Chemicals
At the core of Freya Fusion lies over a decade of regulatory expertise-now elevated by AI. In a landscape defined by complexity and data overload, Freya Fusion brings clarity through automation, connects global teams through unified workflows, and drives innovation with future-ready technology. Know More
