Skip to content

+358 20 7446 800 

  • English
  • Suomi

Search

Show search form

Medfiles
  • Company
    • About us
    • History
    • Medfiles’ team leaders
    • Management team
  • Our Services
        • Human Medicines
          • Regulatory Affairs
            • CMC
            • New Marketing Authorisations
            • Marketing Authorisation Maintenance
            • Local Regulatory Affairs
          • Pharmacovigilance
            • PV System Set Up
            • Post-Authorisation
            • ICSR
            • QPPV
            • Medical Information
          • Clinical Trials
            • Clinical Trial Safety
        • Veterinary Medicines
          • Marketing Authorisation & PV Readiness
          • Regulatory Affairs
            • CMC
            • New Marketing Authorisations
            • Marketing Authorisation Maintenance
            • Local Regulatory Affairs
          • Pharmacovigilance
            • PV System Set Up
            • Post-Authorisation
            • Adverse Event Prosessing
            • QPPV
        • Medical Device & IVDS
          • Quality & Regulatory
            • QMS
            • Technical Documentation
            • Clinical and Performance Evaluations
            • Registrations
            • Post-Market Services
            • Labelling, Translations & Marketing Materials
          • Clinical Investigations and Performance Studies
          • Post-Authorisation & Clinical Vigilance
        • Drug-device combinations
          • Strategy and classification
          • Development, documentation and regulatory alignment
          • Clinical trials and investigations
          • CMC
          • Approvals and conformity
          • Safety & PMS
          • Lifecycle management
        • Food
          • Novel Foods
          • GRAS, NDI and FAP
          • Health Claims
          • Food and Food Supplement Labelling and Marketing Materials
          • FSGs and FSMPs
          • Regulatory Positioning and Strategies
          • Clinical Studies
        • Feed
          • Regulatory Positioning and Strategies
          • Feed Material and Additive Registrations
          • GRAS and FAP
          • Labelling and Marketing Materials
          • Feed for Particular Nutritional Purposes
  • Insights
  • Careers
  • Contact us
    • Contact form
    • Contact our units
    • Offices
    • Invoicing

Service: Veterinary regulatory affairs

  • Meet Medfiles experts at EuroTier 2026

    21.09.2026

    Medfiles at EuroTier 2026
  • Flexible regulatory outsourcing: choosing the level of support that fits your needs

    22.07.2026

    Flexible regulatory outsourcing: choosing the level of support that fits your needs
  • Best practices for managing veterinary variations under Regulation (EU) 2019/6: VNRA, VRA and worksharing explained

    29.06.2026

    Expert services for veterinary medicines
  • Best practices for QRD updates of PI texts of veterinary medicines, QRD template 9.1

    26.06.2026

    QRD template 9.1
  • Repurposing human medicines for veterinary use: Key considerations under EU Regulation 2019/6

    25.06.2026

    Repurposing human medicines for veterinary use Key considerations under EU Regulation 20196
  • New EU veterinary GMP regulations: is your quality system clearly demonstrable

    16.06.2026

    New EU veterinary GMP regulations: is your quality system clearly demonstrable
  • 3 trends affecting the animal health industry in 2026

    14.04.2026

    3 trends affecting the animal health industry in 2026
  • How companies developing human and veterinary medicines can benefit from SME status in the EU

    03.09.2025

    SME status
  • Vetcare & Medfiles: Working together on the maintenance of marketing authorisations and pharmacovigilance of veterinary medicines

    07.04.2025

1 2 Next
Medfiles - Securing a healthier tomorrow

© 2026 Copyright Medfiles.
All rights reserved.

Privacy Policy
Notification Channel

WDB Group

Services

Human medicine
Veterinary medicine
Medical Device & IVD
Drug-device combinations
Food
Feed

Contact

Rajatorpantie 41 C, FI-01640 Vantaa, Finland
VAT: FI10475691

+358 20 7446 800

Contact form
Subscribe to our Newsletter

© 2026 Medfiles • Built with GeneratePress