Skip to main content

Consult

Contact Us

What are you looking for?

Get in Touch

Consult

Missing webform.

  • Your Regulatory Impact Assessment Agent for Turning Change into Action
  • Watch Ria in Action  
.
Home
  • Get in Touch
  •  
  •  
  •  
  •  
  • Home
  • Solutions
    • Back
    • Solutions
    • Medicinal Products
      • Back
      • Medicinal Products Regulatory Services

        Regulatory Affairs
        Regulatory Operations
        Regulatory Medical Writing
        Regulatory Pharmacovigilance
        Medical and Scientific Communication
        Compliance, Audit, and Validation
        Regulatory Artwork Solutions
        Global Regulatory Intelligence
        • MPR - Regulatory Affairs Menu Block
          • Market Access with end-to-end Regulatory Solutions
          • 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
        • MPR - Regulatory Operations Menu
          • Regulatory Publishing and Submissions
          • Regulatory Labeling Services
        • MPR - Medical Writing Menu Block
          • Clinical Services
          • Non-Clinical Writing Services
          • Regulatory Toxicology Services
          • Clinical and Non-Clinical Consulting and Strategic Services
          • Automation in Medical Writing
        • MPR - Pharmacovigilance Menu Block
          • Medical Literature Monitoring
          • Individual Case Safety Report
          • Aggregate Safety Reports
          • Pharmacovigilance Risk Management Plan
          • Pharmacovigilance (PV) Signal Detection Services
          • Pharmacovigilance (PV) Audit Services
          • Quality Control in Pharmacovigilance
          • Qualified Person for Pharmacovigilance
          • Regulatory Intelligence in Pharmacovigilance
          • Pharmacovigilance (PV) Safety Database Services & Solutions
        • MPR - Medical & Scientific Communication Menu Block
          • Medical Copywriting Services
          • Medical and Scientific Writing Services
          • Medical and Scientific Publication Services
          • Creative Scientific Design Studio
          • Promotional Materials MLR Review
          • Medical and Scientific Content Management
          • FDA Ad Promo Submission Services - OPDP 2253
        • MPR - Compliance and Audit Services Menu Block
          • Pharma Quality and Compliance Services
          • 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
        • MPR - New Regulatory Artwork Solutions Menu Block
          • Regulatory Artwork Services

          MPR - Artwork Menu Block
          • Artwork Graphic Studio
          • Artwork Proofreading
          • Global Artwork Translation
          • Artwork Process Consultancy
          • Printed Packaging Print-Proof Quality Check
          • Content to Carton
          • Artwork Lifecycle Coordination
        • MPR - GRI Menu Blocks
          • Global Regulatory Intelligence

    • Medical Devices
      • Back
      • Medical Devices Regulatory Services

        Digital Health / SaMD
        Market Access
        Post Market Surveillance
        EU Compliance
        Clinical & Performance Evaluation
        Quality, Compliance, & Audit
        Artwork Services
        Regulatory Affairs
        Global Regulatory Intelligence
        • MDV - Digital Health/SaMD services menu block
          • SaMD Registration in the US
          • SaMD Registration in the EU
          • Global Market Expansion for SaMD
          • Regulatory Strategy Consultation for SaMD
          • Quality Management Systems Implementation
        • MDV - Market Access menu block
          • Device Registration Americas
          • Device Registration Europe
          • Device Registration China
          • Device Registration South Korea
          • Device Registration Australia
          • Device Registration UK
          • Device Registration Switzerland
          • Device Registration: Rest of the World
          • In-Country Representation
        • MDV - Post Market Surveillance Menu Block
          • Medical Device Complaint Handling
          • PMS Plan (PMSP) and PMS Report (PMSR) for Medical Devices
          • Periodic Safety Update Report (PSUR) for Medical Devices and IVDs
          • Medical Device Recall Management
          • Health Hazard Evaluation
          • Medical Device Translation Services
          • Post-Market Clinical Follow-Up (PMCF) for Medical Devices
        • EU Compliance MDV menu Block
          • CE Marking
          • EU MDR
          • EU IVDR
          • European Authorized Representative
        • MDV Medical Writing Services Menu Block
          • Clinical Evaluation
          • Performance Evaluation
          • Lifecycle Management
          • Literature Search Protocol and Review
        • MDV - Quality Management System services menu block
          • QMS Consultancy Services
          • ISO 14971 Risk Management Consulting
          • QMS Remediation for Medical Devices
          • QMS Compliance and Audit Services 
          • Document Management
          • Corrective and Preventive Action Management Services
          • Supplier Evaluation
        • MDV - new Artwork Services menu Block
          • Regulatory Artwork
        • MDV - Regulatory affairs services menu block
          • Regulatory Mergers & Acquisition Services
          • 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
          • Biocompatibility Services for Medical Devices
        • MDV - GRI Menu Blocks
          • Global Regulatory Intelligence

    • Cosmetics
      • Back
      • Cosmetics Regulatory Services

        COS - Cosmetics services1 Menu
        • Cosmetic Product Labeling Review
        • Cosmetic Safety Assessment and Toxicology Services
        • Global Regulatory Compliance and Consulting (GRCC)
        • Formulation and Ingredient Review
        • Cosmetic Product Information File (PIF)
        • Modernization of the Cosmetics Regulation Act of 2022 (MoCRA)
        • Go-to-market and Legal Representative (LR)
        • EUDR Compliance Services for Cosmetics Industry
        COS - Cosmetics services2 Menu
        • Comprehensive Artwork Services for Cosmetics
        • Global Cosmetovigilence Services
        • Claims Review
        • Cosmetic Testing Services
        • Cosmetic Regulatory Intelligence
        • Global Regulatory Intelligence

    • Food Supplements
      • Back
      • Food Supplements Regulatory Services
        Food Product Service

        FDS - Food Product Service menu
        • Food & Food Supplements Product Services
        • Food and Food Supplements Artwork Services
        • Global Regulatory Compliance and Consulting (GRCC)
        • 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

        Food Product Compliance

        FDS - Food Product Compliance Menu
        • 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

        Novel Food Registration

    • Chemicals
      • Back
      • Chemicals Regulatory Services

        CSRA - Chemicals service1 Menu
        • Extended Safety Data Sheet (eSDS) Services
        • Global Regulatory Compliance and Consulting (GRCC)
        • Chemical Data Scouting
        • Chemical Scientific Assessment Reports and Position Paper Report
        • Supply Chain Regulatory Compliance
        • Chemical Packaging Regulations
        • Global Biocidal Products Regulation Services
        • Regulation of Tobacco Products
        • Ecolabeling Regulatory Support
        • Chemical Safety Data Sheet (SDS) Authoring & Compliance Services
        • Household and Chemical Products Artwork Services
        • Sustainability Consulting Services
        CSRA - Chemicals service2 Menu
        • Retail Due Diligence, Compliance & Clearance-to-Market Services for Consumer Products
        • 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
        • Environmental Risk Assessment (ERA) Services
        • Global Regulatory Intelligence
        • EU Poison Centre Notification (PCN)
        • EU Detergents Regulation (EU) 2026/405
        • LHAMA Compliance Services: US Art Materials Regulation & ASTM D-4236 Compliance

    • Spotlight
      • Back
      • Spotlight
        • EUDR Compliance | Food, Cosmetics & Chemicals
        • EUDR Knowledge Hub
  • Global
    • Back
    • Global
    • Americas
      • Back
      • Americas
      • Mobile Menu Americas
        • Argentina
        • Bolivia
        • Brazil
        • Canada
        • Chile
        • Colombia
        • Costa Rica
        • Dominican Republic
        • Guatemala
        • Mexico
        • Panama
        • Paraguay
        • Peru
        • Puerto Rico
        • United States
        • Venezuela
    • Europe
      • Back
      • Europe
      • Mobile Menu Eupope
        • Albania
        • Austria
        • Belarus
        • Belgium
        • Bulgaria
        • Croatia
        • Cyprus
        • Czech Republic
        • Denmark
        • Estonia
        • European Union
        • Finland
        • France
        • Germany
        • Greece
        • Hungary
        • Ireland
        • Italy
        • Kazakhstan
        • Kosovo
        • Latvia
        • Lithuania
        • Luxembourg
        • Macedonia
        • Malta
        • Netherlands
        • Norway
        • Poland
        • Portugal
        • Romania
        • Serbia
        • Slovakia
        • Slovenia
        • Spain
        • Sweden
        • Switzerland
        • United Kingdom
        • Uzbekistan
    • Asia - Pacific
      • Back
      • Asia - Pacific
      • Mobile Menu Asia - Pacific
        • Australia
        • Bangladesh
        • Cambodia
        • China
        • Hong Kong
        • India
        • Indonesia
        • Japan
        • Malaysia
        • New Zealand
        • Pakistan
        • Philippines
        • Singapore
        • South Korea
        • Sri Lanka
        • Taiwan
        • Thailand
        • Vietnam
    • Africa & Middle East
      • Back
      • Africa & Middle East
      • Mobile Menu Africa & Middle East
        • Algeria
        • Bahrain
        • Botswana
        • Egypt
        • Ethiopia
        • Ghana
        • Iraq
        • Israel
        • Jordan
        • Kenya
        • Kuwait
        • Lebanon
        • Morocco
        • Nigeria
        • Oman
        • Qatar
        • Saudi Arabia
        • South Africa
        • Tunisia
        • Turkey
        • UAE
        • Uganda
        • Yemen
        • Zimbabwe
  • Customers
    • Back
    • Customers
    • Mobile Menu Customers
      • Success Stories
      • Case Studies
      • Testimonials
  • Insights
    • Back
    • Insights
    • Mobile Menu Insights
      • Blogs
      • Brochures
      • Infographics
      • Webinars
      • Freyr Podcasts
      • What is ...?
      • White Papers
      • Fireside Chats
      • e-Books
      • Global Health Authority Mandates
      • Regulatory Roundup
      • Templates and Checklists
      • Industry News
      • Videos
      • Toolkits
  • Company
    • Back
    • Company
    • Mobile Menu Company
      • About Us
      • Awards & Recognitions
      • Press Releases
      • Thought Leadership Articles
      • Freyr in Media
      • Industry Events
      • Freyr Events
      • Careers
      • Compliance Wall
      • Corporate Social Responsibility
      • Functional Delivery Models
      • Partner with Us
      • Contact Us
  •   English

    en USA (English) en Canada (French) fr France (French) IT Italy (Italian) es Spain (Spanish) ge Germany (German) pt Portugal (Portuguese) pl Poland (Polish)

    Japan Japan (Japanese)  Korea Korea (Korean)  Mexico Mexico (Spanish)  China China (Chinese)  Colombia Colombia (Spanish)  Brazil Brazil (Portuguese)  Australia Australia (English)  Sri Lanka Sri Lanka (English)  India India (English)  Malaysia Malaysia (English)  Nigeria Nigeria (English)  Saudi Arabia Saudi Arabia (English)  Thailand Thailand (English) 
  • Solutions
    Medicinal Products
    Medical Devices
    Consumer
    freya fusion
    Medicinal Products Regulatory Services
    Regulatory Affairs
    Regulatory Operations
    Regulatory Medical Writing
    Regulatory Pharmacovigilance
    Medical and Scientific Communication
    Compliance, Audit, and Validation
    Regulatory Artwork Solutions
    Global Regulatory Intelligence
    • MPR - Regulatory Affairs Menu Block
      • Market Access with end-to-end Regulatory Solutions
      • 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
    • MPR - Regulatory Operations Menu
      • Regulatory Publishing and Submissions
      • Regulatory Labeling Services
    • MPR - Medical Writing Menu Block
      • Clinical Services
      • Non-Clinical Writing Services
      • Regulatory Toxicology Services
      • Clinical and Non-Clinical Consulting and Strategic Services
      • Automation in Medical Writing
    • MPR - Pharmacovigilance Menu Block
      • Medical Literature Monitoring
      • Individual Case Safety Report
      • Aggregate Safety Reports
      • Pharmacovigilance Risk Management Plan
      • Pharmacovigilance (PV) Signal Detection Services
      • Pharmacovigilance (PV) Audit Services
      • Quality Control in Pharmacovigilance
      • Qualified Person for Pharmacovigilance
      • Regulatory Intelligence in Pharmacovigilance
      • Pharmacovigilance (PV) Safety Database Services & Solutions
    • MPR - Medical & Scientific Communication Menu Block
      • Medical Copywriting Services
      • Medical and Scientific Writing Services
      • Medical and Scientific Publication Services
      • Creative Scientific Design Studio
      • Promotional Materials MLR Review
      • Medical and Scientific Content Management
      • FDA Ad Promo Submission Services - OPDP 2253
    • MPR - Compliance and Audit Services Menu Block
      • Pharma Quality and Compliance Services
      • 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
    • MPR - New Regulatory Artwork Solutions Menu Block
      • Regulatory Artwork Services

      MPR - Artwork Menu Block
      • Artwork Graphic Studio
      • Artwork Proofreading
      • Global Artwork Translation
      • Artwork Process Consultancy
      • Printed Packaging Print-Proof Quality Check
      • Content to Carton
      • Artwork Lifecycle Coordination
    • MPR - GRI Menu Blocks
      • Global Regulatory Intelligence
    Medical Devices Regulatory Services
    Digital Health / SaMD
    Market Access
    Post Market Surveillance
    EU Compliance
    Clinical & Performance Evaluation
    Quality, Compliance, & Audit
    Artwork Services
    Regulatory Affairs
    Global Regulatory Intelligence
    • MDV - Digital Health/SaMD services menu block
      • SaMD Registration in the US
      • SaMD Registration in the EU
      • Global Market Expansion for SaMD
      • Regulatory Strategy Consultation for SaMD
      • Quality Management Systems Implementation
    • MDV - Market Access menu block
      • Device Registration Americas
      • Device Registration Europe
      • Device Registration China
      • Device Registration South Korea
      • Device Registration Australia
      • Device Registration UK
      • Device Registration Switzerland
      • Device Registration: Rest of the World
      • In-Country Representation
    • MDV - Post Market Surveillance Menu Block
      • Medical Device Complaint Handling
      • PMS Plan (PMSP) and PMS Report (PMSR) for Medical Devices
      • Periodic Safety Update Report (PSUR) for Medical Devices and IVDs
      • Medical Device Recall Management
      • Health Hazard Evaluation
      • Medical Device Translation Services
      • Post-Market Clinical Follow-Up (PMCF) for Medical Devices
    • EU Compliance MDV menu Block
      • CE Marking
      • EU MDR
      • EU IVDR
      • European Authorized Representative
    • MDV Medical Writing Services Menu Block
      • Clinical Evaluation
      • Performance Evaluation
      • Lifecycle Management
      • Literature Search Protocol and Review
    • MDV - Quality Management System services menu block
      • QMS Consultancy Services
      • ISO 14971 Risk Management Consulting
      • QMS Remediation for Medical Devices
      • QMS Compliance and Audit Services 
      • Document Management
      • Corrective and Preventive Action Management Services
      • Supplier Evaluation
    • MDV - new Artwork Services menu Block
      • Regulatory Artwork
    • MDV - Regulatory affairs services menu block
      • Regulatory Mergers & Acquisition Services
      • 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
      • Biocompatibility Services for Medical Devices
    • MDV - GRI Menu Blocks
      • Global Regulatory Intelligence
    Consumers
    Cosmetics
    Food Supplements
    Chemicals
    Spotlight
    • COS - Cosmetics services1 Menu
      • Cosmetic Product Labeling Review
      • Cosmetic Safety Assessment and Toxicology Services
      • Global Regulatory Compliance and Consulting (GRCC)
      • Formulation and Ingredient Review
      • Cosmetic Product Information File (PIF)
      • Modernization of the Cosmetics Regulation Act of 2022 (MoCRA)
      • Go-to-market and Legal Representative (LR)
      • EUDR Compliance Services for Cosmetics Industry
      COS - Cosmetics services2 Menu
      • Comprehensive Artwork Services for Cosmetics
      • Global Cosmetovigilence Services
      • Claims Review
      • Cosmetic Testing Services
      • Cosmetic Regulatory Intelligence
      • Global Regulatory Intelligence
    • FDS - Service1 Menu block
      • Food & Food Supplements Product Services
      • Food and Food Supplements Artwork Services
      • Global Regulatory Compliance and Consulting (GRCC)
      • 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
      FDS Categories Supported menu block
      • Categories Supported
      • Cultured Food Products Regulatory Compliance for (Animal & Plant-Based)
      • Dietary Supplement Regulation and Compliance
      • Ensure Global Compliance for Your Tobacco and Nicotine Products
      • Herbal Supplements (Botanical Extracts)
      • Infant Formula Regulatory Compliance
      • Medical Foods / FSMP
      • Organic Foods
      • Probiotics, Prebiotics, Postbiotics & Synbiotics
      • Processed Food Products
      • Traditional Medicines Regulatory Compliance
      • Alcoholic Beverages
      FDS - Service2 Menu block
      • 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

      Global Regulatory Intelligence

    • CSRA - Chemicals service1 Menu
      • Extended Safety Data Sheet (eSDS) Services
      • Global Regulatory Compliance and Consulting (GRCC)
      • Chemical Data Scouting
      • Chemical Scientific Assessment Reports and Position Paper Report
      • Supply Chain Regulatory Compliance
      • Chemical Packaging Regulations
      • Global Biocidal Products Regulation Services
      • Regulation of Tobacco Products
      • Ecolabeling Regulatory Support
      • Chemical Safety Data Sheet (SDS) Authoring & Compliance Services
      • Household and Chemical Products Artwork Services
      • Sustainability Consulting Services
      CSRA - Chemicals service2 Menu
      • Retail Due Diligence, Compliance & Clearance-to-Market Services for Consumer Products
      • 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
      • Environmental Risk Assessment (ERA) Services
      • Global Regulatory Intelligence
      • EU Poison Centre Notification (PCN)
      • EU Detergents Regulation (EU) 2026/405
      • LHAMA Compliance Services: US Art Materials Regulation & ASTM D-4236 Compliance
      • EUDR Compliance | Food, Cosmetics & Chemicals
      • EUDR Knowledge Hub

      •  

    Freya Fusion

    Via: Variation Identification Agent

    Ria: Regulatory Impact Assessment Agent

    Stay Ahead with a Unified, AI-First Regulatory Cloud

    freya fusion is Freyr’s flagship AI-first regulatory platform, designed to meet complex, real-world compliance needs. Grounded in 15+ years of regulatory expertise and driven by advanced AI/ML. freya fusion is a unified ecosystem that empowers RIM and covers the entire regulatory lifecycle - from registrations and submissions to labeling, artwork, intelligence, and change control. Know More

    • Consumer
    • Medicinal products
      • Regulatory Affairs Services
        • Market Access with end-to-end Regulatory Solutions
        • Drug Development Regulatory Services
          • Pre-submission Meetings/HA Interactions
          • Clinical Trial Applications
        • Regulatory Strategy and Insights
          • Regulatory Strategy Consulting
          • Regulatory Submission Roadmaps/Regulatory Intelligence
          • Regulatory Staffing Services
          • Global Regulatory Affairs Services
          • Gap Analysis
          • Artificial Intelligence (AI)-powered Regulatory Services
        • Dossier Authoring
          • CTD Templates
          • Biologics Registration Services
        • Post Approval/Lifecycle Management
          • Post-Approval Change Submissions
          • Nitrosamine impurity Risk Assessment
          • Lifecycle Management
        • Country-specific Regulatory Services
        • Global Health Authorities - Specific Services
          • USFDA
            • Abbreviated New Drug Application Submissions
            • Biologics License Applications Submission
            • Drug Master File (DMF) Submissions
            • New Drug Application Submission
            • Investigational New Drug Applications
            • Nitrosamine Impurity Risk Assessment
          • Health Canada
            • Abbreviated New Drug Submission
            • New Drug Submission
            • Clinical Trial Application (CTA) Submissions
            • Drug Master File (DMF) Submissions
          • European
            • Active Substance Master File Submissions
            • Centralised Procedure
            • Certification of Suitability
            • Decentralized Procedure
            • EU Marketing Authorization Application
            • Investigational Medicinal Product Dossier
            • Mutual Recognition Procedure (MRP)
            • National Procedure (NP)
        • EU CTR Submissions
      • Regulatory Operations
        • Regulatory Publishing and Submissions
          • AI-powered Regulatory
          • Global eCTD Publishing and Submission Services
          • NeeS Submissions
          • Paper Submissions
          • CSR - Report-Level Publishing
          • Legacy Conversions
          • AD promo submission services
          • Archiving Services for Regulatory Publishing and Submission
          • Regulatory Data Migration Services
          • Regulatory Document Formatting Services
          • Submission QC Automation
          • Auto Document Level Publishing
        • Regulatory Labeling Services
          • Strategic Labeling Consulting
            • Process Consulting
            • Technology Consulting
            • Content Harmonization & Standardization
            • Go-to-market Labeling Strategies
          • Labeling Translation
            • Translation Creation & Updation
            • Translation Quality Check
            • Translation Coordination
          • Regional Labeling
            • USPI Preparation
            • EU Labeling
            • ROW Labeling
            • Linguistic Review
            • SPL/SPM (Creation & Updation)
            • Competitor Label Analysis
            • Label Comparison
            • Monitoring Reference Label Changes
            • Readability Test
          • Global Labeling
            • CCDS/CSI Creation & Updation
            • Monitoring CCDS Change implementation and Deviation Management
            • Local Justification Document Preparation
          • Clinical Labeling
            • Target Product Profiling (TPP)
            • Developmental CCDS Creation & Updation
          • Labeling Automation
            • Labeling Content Management
            • Labeling Templatization
            • Large-volume Change Automation
            • End-to-end Tracking
            • e-labeling
          • AI-powered Regulatory Labeling Services
          • Pharma Labeling Compliance
      • Regulatory Artwork Solutions
        • Regulatory Artwork Services
          • Artwork Graphic Studio
            • Packaging Artwork Mock-up Creation
            • Changes to Existing Artwork
            • Private Label Artwork for Pharma
          • Artwork Proofreading
          • Global Artwork Translation
          • Artwork Process Consultancy
          • Printed Packaging Print-Proof Quality Check
          • Content to Carton
          • Artwork Lifecycle Coordination
            • End-to-End Artwork Workflow Coordination
      • Pharmacovigilance
        • Medical Literature Monitoring
        • Individual Case Safety Report
        • Aggregate Safety Reports
        • Pharmacovigilance Risk Management Plan
        • Pharmacovigilance (PV) Signal Detection Services
        • Pharmacovigilance (PV) Audit Services
        • Quality Control in Pharmacovigilance
        • Qualified Person for Pharmacovigilance
        • Regulatory Intelligence in Pharmacovigilance
        • Pharmacovigilance (PV) Safety Database Services & Solutions
      • Medical Writing
        • Clinical Services
          • Regulatory Writing Services
          • Clinical Trial and Consulting Services
          • Clinical Trial Audit and Monitoring Services
          • Quality Check and Medical Review of Regulatory Documents
          • Risk-Benefit Analysis
          • Clinical Data Transparency Initiative
        • Non-Clinical Writing Services
        • Regulatory Toxicology Services
          • ADE/PDE Determination/Report Services
          • F-Value Reports for Child Resistant Packaging (CRP)
          • Toxicological Risk Assessment (TRA) of Impurities, Extractables and Leachables
          • Environmental Risk Assessment (ERA) of Medicinal Products
        • Clinical and Non-Clinical Consulting and Strategic Services
          • Clinical Writing Consulting and Strategic Services
          • Technical Writing Support for GxP Compliance
          • Business Process Optimization
          • Non-clinical Consulting & Strategic Services
        • Automation in Medical Writing
          • Narrative writing tool
          • Literature review tool
          • Quality review tool
          • End-to-End Medical Writing Services
      • Compliance and Audit Services
        • Pharma Quality and Compliance Services
        • SOP Writing and SOP Review Services
        • Pharma GxP Audit Services
          • Remote and Virtual Audits
        • Pharma CSV and CSA Services
        • QMS Remediation and Establishment Services
        • End-to-end Regulatory Compliance Services
      • Medical and Scientific Communication
        • Medical Copywriting Services
        • Medical and Scientific Writing Services
        • Medical and Scientific Publication Services
        • Creative Scientific Design Studio
        • Promotional Materials MLR Review
        • Medical and Scientific Content Management
        • FDA Ad Promo Submission Services - OPDP 2253
      • Global Regulatory Intelligence
        • Global Regulatory Intelligence
      • Generics
        • USFDA
          • Abbreviated New Drug Application
          • ANDA Refuse-to-Receive Practices
          • Due Diligence Assessment of ANDA
          • US FDA Health Authority Interactions
          • Pre-ANDA Submissions
          • Competitive Generic Therapies Designation
          • Product Development Strategy for Generic Drug
          • ANDA Post-approval Changes
          • Drug Master File (DMF) Submission
          • Change Control Assessment and Change Submission Strategy
          • ANDA Pre-Submission Facility Correspondence
          • Gap Analysis and Authoring
          • Publishing and Submission
          • US FDA Query Management (IRs/ DRLs/ CRLs)
        • EU- EMA
          • MAA Approval Support
          • MAA Registration
          • Health Authority Interactions in Europe
          • ASMF/CEP Submissions
          • Post-approval Changes to Drug Substance
          • MAH/QP/QPPV Requirements
          • Sunset Clause
          • Submission Slot Booking
          • Hybrid Applications
          • Renewals Submissions
          • Gap Analysis and Authoring
          • Publishing and Submission
          • Change Control Evaluation and Variation Submission Strategies
        • Health Canada
          • Regulatory Strategic Guidance
          • Health Canada ANDS
          • Health Canada Drug Master File (DMF) Submission
          • Change Control Evaluation and Submission Strategy
          • ANDA Post-approval Change Submissions
          • Canada Health Authority Interactions
          • Health Canada Query Management
        • Our Capabilities
          • Ensuring 'Right Opportunities' for 'Right Market'
          • Breaking complex generics Regulatory Challenges
          • Generic Application Expertise
          • Drug Master File (DMF) Submissions Expertise
          • First-to-File Generics
          • FAQs on Generics
      • Innovators
        • Our Regulatory Services
          • Biologics License Application (BLA)
          • Clinical Trial Applications (CTAs)
          • Investigational Medicinal Product Dossier
          • Investigational New Drug Applications
          • New Drug Applications
          • New Drug Submissions
        • Cross-functional specialty
          • Clinical Labeling
          • Clinical Trial Monitoring
          • DMF Capabilities
          • Toxicological Risk Assessment
          • Publishing and Submission Competencies
          • Regulatory Labeling Competencies
          • Regulatory Medical Writing Competencies
          • Regulatory Strategy Consulting Competencies
          • Artwork competencies
        • Regional Expertise
          • Regional Expertise
        • Freyr as a Partner from Discovery Stage
          • Freyr as a Partner from Discovery Stage
    • Medical Devices
      • Market Access
        • Device Registration Americas
          • USA
            • e-Star
            • 513(g)
            • 510(k)
            • Q-submission
            • Pre-market Approval
            • RFD & Pre-RFD
            • UDI and GUDID Solutions for the FDA Compliance
          • Canada
            • Canada ISED Representative Service
            • Medical Device Establishment Licence (MDEL) Solutions for Canada
            • Medical Device Importer Solutions for Compliance in Canada
            • Medical Device Licence (MDL) Solutions for Canada
        • Device Registration Europe
          • CE Marking
          • EU MDR
          • EU IVDR
          • European Authorized Representative
        • Device Registration China
        • Device Registration South Korea
        • Device Registration Australia
        • Device Registration UK
        • Device Registration Switzerland
        • Device Registration: Rest of the World
        • In-Country Representation
          • Australian TGA Sponsor
          • Korean Registration Holder (KRH)
          • Mexican Registration Holder (MRH)
          • US Agent
          • Swiss Authorised Representative (CH-Rep)
          • UK Responsible Person (UKRP)
          • Designated Market Authorization Holder (DMAH)
          • China Agent Services
          • Brazil Registration Holder (BRH)
          • Indian Authorization Agent for Medical Device Registration in India
          • In-country representation Rest of the world
      • Post Market Surveillance
        • Medical Device Complaint Handling
        • PMS Plan (PMSP) and PMS Report (PMSR) for Medical Devices
        • Periodic Safety Update Report (PSUR) for Medical Devices and IVDs
        • Medical Device Recall Management
        • Health Hazard Evaluation
        • Medical Device Translation Services
        • Post-Market Clinical Follow-Up (PMCF) for Medical Devices
      • Medical Writing for Medical Devices
        • Clinical Evaluation
          • Clinical Evaluation Plan (CEP)
          • Clinical Evaluation Report (CER)
        • Performance Evaluation
          • Scientific Validity Report (SVR)
          • Clinical Performance Report (CPR)
          • Analytical Performance Report (APR)
          • Performance Evaluation for In Vitro Diagnostic Medical Devices
          • Performance EvaluationReport (PER) IVDR
        • Lifecycle Management
        • Literature Search Protocol and Review
      • Regulatory Affairs
        • Regulatory Mergers & Acquisition Services
        • Device Documentation
          • Device History File
          • Device Technical File Publishing
        • Labeling Services
        • Technical Writing Services
        • RA Staff Augementation Services
        • Regulatory Consulting
          • Life cycle management
          • Medical Device Consulting
          • IVD Consulting
          • SaMD Consulting
          • Combination product Consulting
          • Regulatory Intelligence
          • Device classification & Categorization
        • Human Factors Engineering for Medical Devices
        • Market Intelligence Service
        • Medical and Scientific Communication
        • Biocompatibility Services for Medical Devices
      • Quality Management System (QMS)
        • QMS Consultancy Services
        • ISO 14971 Risk Management Consulting
        • QMS Remediation for Medical Devices
        • QMS Compliance and Audit Services 
        • Document Management
        • Corrective and Preventive Action Management Services
        • Supplier Evaluation
      • Digital Health/SaMD
        • SaMD Registration in the US
        • SaMD Registration in the EU
        • Global Market Expansion for SaMD
        • Regulatory Strategy Consultation for SaMD
        • Quality Management Systems Implementation
      • Artwork Services
        • Regulatory Artwork
      • Global Regulatory Intelligence
        • Global Regulatory Intelligence
    • Cosmetics
      • Cosmetics Services
        • Cosmetic Product Labeling Review
        • Cosmetic Safety Assessment and Toxicology Services
        • Global Regulatory Compliance and Consulting (GRCC)
        • Formulation and Ingredient Review
        • Cosmetic Product Information File (PIF)
        • Modernization of the Cosmetics Regulation Act of 2022 (MoCRA)
        • Go-to-market and Legal Representative (LR)
        • EUDR Compliance Services for Cosmetics Industry
      • Cosmetics Service
        • Comprehensive Artwork Services for Cosmetics
        • Global Cosmetovigilence Services
        • Claims Review
        • Cosmetic Testing Services
        • Cosmetic Regulatory Intelligence
        • Global Regulatory Intelligence
    • Food Supplements
      • Food & Food Supplements Product Services
        • Food & Food Supplements Product Services
        • Food and Food Supplements Artwork Services
        • Global Regulatory Compliance and Consulting (GRCC)
        • 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
      • Sustainability Services
        • 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
      • Categories Supported
        • Categories Supported
        • Cultured Food Products Regulatory Compliance for (Animal & Plant-Based)
        • Dietary Supplement Regulation and Compliance
        • Ensure Global Compliance for Your Tobacco and Nicotine Products
        • Herbal Supplements (Botanical Extracts)
        • Infant Formula Regulatory Compliance
        • Medical Foods / FSMP
        • Organic Foods
        • Probiotics, Prebiotics, Postbiotics & Synbiotics
        • Processed Food Products
        • Traditional Medicines Regulatory Compliance
        • Alcoholic Beverages
    • Chemicals
      • CSRA Services
        • Extended Safety Data Sheet (eSDS) Services
        • Global Regulatory Compliance and Consulting (GRCC)
        • Chemical Data Scouting
        • Chemical Scientific Assessment Reports and Position Paper Report
        • Supply Chain Regulatory Compliance
        • Chemical Packaging Regulations
        • Global Biocidal Products Regulation Services
        • Regulation of Tobacco Products
        • Ecolabeling Regulatory Support
        • Chemical Safety Data Sheet (SDS) Authoring & Compliance Services
        • Household and Chemical Products Artwork Services
        • Sustainability Consulting Services
      • CSRA Services
        • Retail Due Diligence, Compliance & Clearance-to-Market Services for Consumer Products
        • 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
        • Environmental Risk Assessment (ERA) Services
        • Global Regulatory Intelligence
        • EU Poison Centre Notification (PCN)
        • EU Detergents Regulation (EU) 2026/405
        • LHAMA Compliance Services: US Art Materials Regulation & ASTM D-4236 Compliance
  • Global
    Americas
    Europe
    Asia-Pacific
    Africa & Middle East
    Global Americas Menu Block
    • Argentina
    • Bolivia
    • Brazil
    • Canada
    • Chile
    • Colombia
    • Costa Rica
    • Dominican Republic
    • Guatemala
    • Mexico
    • Panama
    • Paraguay
    • Peru
    • Puerto Rico
    • United States
    • Venezuela
    Global Europe Menu Block
    • Albania
    • Austria
    • Belarus
    • Belgium
    • Bulgaria
    • Croatia
    • Cyprus
    • Czech Republic
    • Denmark
    • Estonia
    • European Union
    • Finland
    • France
    • Germany
    • Greece
    • Hungary
    • Ireland
    • Italy
    • Kazakhstan
    • Kosovo
    • Latvia
    • Lithuania
    • Luxembourg
    • Macedonia
    • Malta
    • Netherlands
    • Norway
    • Poland
    • Portugal
    • Romania
    • Serbia
    • Slovakia
    • Slovenia
    • Spain
    • Sweden
    • Switzerland
    • United Kingdom
    • Uzbekistan
    Global Asia - Pacific Menu Block
    • Australia
    • Bangladesh
    • Cambodia
    • China
    • Hong Kong
    • India
    • Indonesia
    • Japan
    • Malaysia
    • New Zealand
    • Pakistan
    • Philippines
    • Singapore
    • South Korea
    • Sri Lanka
    • Taiwan
    • Thailand
    • Vietnam
    Global Africa & Middle East Menu Block
    • Algeria
    • Bahrain
    • Botswana
    • Egypt
    • Ethiopia
    • Ghana
    • Iraq
    • Israel
    • Jordan
    • Kenya
    • Kuwait
    • Lebanon
    • Morocco
    • Nigeria
    • Oman
    • Qatar
    • Saudi Arabia
    • South Africa
    • Tunisia
    • Turkey
    • UAE
    • Uganda
    • Yemen
    • Zimbabwe
    • Americas
      • Argentina
      • Bolivia
      • Brazil
      • Canada
      • Chile
      • Colombia
      • Costa Rica
      • Dominican Republic
      • Guatemala
      • Mexico
      • Panama
      • Paraguay
      • Peru
      • Puerto Rico
      • United States
      • Venezuela
    • Europe
      • Albania
      • Austria
      • Belarus
      • Belgium
      • Bulgaria
      • Croatia
      • Cyprus
      • Czech Republic
      • Denmark
      • Estonia
      • Finland
      • France
      • Germany
      • European Union
      • Greece
      • Hungary
      • Ireland
      • Italy
      • Kazakhstan
      • Kosovo
      • Latvia
      • Lithuania
      • Luxembourg
      • Macedonia
      • Malta
      • Netherlands
      • Norway
      • Poland
      • Portugal
      • Romania
      • Serbia
      • Slovakia
      • Slovenia
      • Spain
      • Sweden
      • Switzerland
      • United Kingdom
      • Uzbekistan
    • Asia-Pacific
      • Australia
      • Bangladesh
      • Cambodia
      • China
      • Hong Kong
      • India
      • Indonesia
      • Japan
      • Malaysia
      • New Zealand
      • Pakistan
      • Philippines
      • Singapore
      • South Korea
      • Sri Lanka
      • Taiwan
      • Thailand
      • Vietnam
    • Africa & Middle East
      • Algeria
      • Bahrain
      • Botswana
      • Egypt
      • Ethiopia
      • Ghana
      • Iraq
      • Israel
      • Jordan
      • Kenya
      • Lebanon
      • Morocco
      • Oman
      • Kuwait
      • Nigeria
      • Qatar
      • Saudi Arabia
      • South Africa
      • Tunisia
      • Turkey
      • UAE
      • Uganda
      • Yemen
      • Zimbabwe
  • Customers
    • Success Stories
    • Case Studies
    • Testimonials
  • Insights
    • Blogs
    • Brochures
    • Infographics
    • Webinars
    • Freyr Podcasts
    • What is ...?
    • White Papers
    • Fireside Chats
    • e-Books
    • Global Health Authority Mandates
    • Regulatory Roundup
    • Templates and Checklists
    • Industry News
    • Videos
    • Toolkits
  • Company
    • About Us
    • Awards & Recognitions
    • Press Releases
    • Thought Leadership Articles
    • Freyr in Media
    • Industry Events
    • Freyr Events
    • Careers
    • Compliance Wall
    • Corporate Social Responsibility
    • Functional Delivery Models
    • Partner with Us
    • Contact Us
  • Get in Touch

  •  
  •  
    • +1 908 483 7958
    • +44 2037 012379
    • +1 778 308 4671
    • +49 6181 707 9007
    • +52 55 41613365
    • +65 315 894 72
    • +62 604 2250544
    • +91 40 65480999
    • +61 2 8607 5105
    • +41 225 087 129
  •  
    • sales@freyrsolutions.com
    • hr@freyrsolutions.com
  English

en USA (English) en Canada (French) fr France (French) IT Italy (Italian) es Spain (Spanish) ge Germany (German) pt Portugal (Portuguese) pl Poland (Polish)

Japan Japan (Japanese)  Korea Korea (Korean)  Mexico Mexico (Spanish)  China China (Chinese)  Colombia Colombia (Spanish)  Brazil Brazil (Portuguese)  Australia Australia (English)  Sri Lanka Sri Lanka (English)  India India (English)  Malaysia Malaysia (English)  Nigeria Nigeria (English)  Saudi Arabia Saudi Arabia (English)  Thailand Thailand (English) 

Brazil: ANVISA approves new regulatory framework for herbal medicines

December 17, 2025

Consult Now

Source
https://www.gov.br/anvisa/pt-br/assuntos/noticias-anvisa/2025/anvisa-aprova-nov…
Select Mandate HA
ANVISA
Select Mandate Function
Regulatory Affairs

Global Health Authority Mandates

  • Black Triangle Scheme Information for Sponsors
  • EU Pharmacovigilance Regulation (EU) 2025/1466 Now in Effect: Strengthening Pharmacovigilance Compliance Across the EU
  • Egypt Updates Bioequivalence Guideline with ICH M10 and M13A Implementation
  • EMA Revised Compilation of Union Procedures on GMP/GDP Inspections — Updated June 2026
  • EMA Revised EU Variation Guidelines — Mandatory Compliance from 15 January 2026; Type IA Annual Update Deadlines from November 2026
View More

How can we help you?

Please let us know your requirements, and we will contact you.
  +1 908 483 7958
  +44 203 701 2379
  +91 40 65480999
  +27 105 002 556

 sales@freyrsolutions.com


Connect with Us

  •  

  •  
  •  
  •  
Terms of Use | Privacy Policy | Cookie Policy 
© Copyright 2026 Freyr. All Rights Reserved.