Validation of applications for veterinary medicines
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How to make sure an application relating to an authorisation for a veterinary medicine is complete and will pass validation.
Adapted edition
- Document type
- Reference Guide
- Format
- DOCX
- Pages
- 4
- Language
- English
- Version
- 1.0
- Updated
- 2026-09-17
- Category
- Safety & operations
- Licence
- Open Government Licence v3.0
Description
How to make sure an application relating to an authorisation for a veterinary medicine is complete and will pass validation. Consult the original guidance for current legal and operational details.
Contents
- Validation process
- Deferred validation
- Failed validation
- Passed validation
- How to submit a valid application
- Active Substance Master File (ASMF) in support of an application
- New Marketing Authorisations (MAs)
- Good Manufacturing Practice (GMP) Certificates
- Generic and Generic-Hybrid
- Informed Consent (Copycats)
- SRP - Subsequent Recognition Procedure
- Variation applications for MAs and Homeopathic Registrations
- Contact
Source and licence
Veterinary Medicines Directorate
AttributionVeterinary Medicines Directorate, ‘Validation of applications for veterinary medicines’ (updated 5 December 2025), reused under the Open Government Licence v3.0.
ChangesNeutral text-only adaptation from the official GOV.UK Content API body: headings, paragraphs, ordered and unordered list items and clickable source-link destinations in an appendix preserved. Images, logos, page design, accessible-format request widgets and linked attachments excluded; normalised whitespace, invisible format marks and typography.
Version history
- v1.017/09/2026