- Status
- In Force
- Penalty ceiling
- Prosecution 1 of 23 obligations carry an unlimited fine. 1 carries different penalties and 21 have no criminal penalty — flagged in the list below.
Does it bind you?
Business-side roles with duties under this instrument.
Plus 1 duty on the regulator, Crown ministers and public bodies — folded into the section list below.
Other Acts binding the same actors
If a role above is yours, these are the other instruments that most often bind it.
Any Person — also bound by 2340 other Acts
Manufacturer — also bound by 502 other Acts
Applicant — also bound by 307 other Acts
Operator — also bound by 746 other Acts
Trader — also bound by 825 other Acts
Farmer or Animal Keeper — also bound by 80 other Acts
What it requires
Regulations creating concrete business duties or carrying penalties, grouped as the instrument is structured. Titles link to the source text — blue means you’re leaving for legislation.gov.uk.
- Keep transaction records for POM-V, POM-VPS and cascade veterinary medicinesAny Person
- Provide antibiotic sales and usage information when the Secretary of State asksAny Person
- Commit an offence under the Veterinary Medicines RegulationsAny Person
Unlimited fine
- Provide scientific justification for combination active substances in veterinary medicine applicationsApplicant
- Provide study results when bioequivalence cannot be demonstratedApplicant
- Notify the Secretary of State of veterinary medicine shortagesAny Person
- Submit electronic variation applications for marketing authorisationsApplicant
- Operate a pharmacovigilance system for your veterinary medicine productsManufacturer
Other duties (1) — Crown / regulator
- Secretary of State must complete homeopathic remedy registration within 210 daysCrown / Minister / Government department
- Notify and apply for variation before altering premises or key personnelManufacturer
- Verify manufacturer's GMP certificate before importing veterinary medicinesManufacturer
- Comply with manufacturing, quality and notification duties for veterinary medicinesManufacturer
- Operate a pharmaceutical quality system and manage recallsManufacturer
- Get authorisation before manufacturing vet medicines or handling animal blood/stem cellsApplicant
- Prescribe antimicrobials only for the shortest period neededAny Person
- Notify Secretary of State and apply for variation before material changes to wholesale authorisationAny Person
- Meet wholesale veterinary supply, recall, audit and self-inspection dutiesTrader
- Set withdrawal periods ensuring residue limits are not exceededManufacturer
- Do not promote or facilitate unauthorised cascade useAny Person
- Mix medicinal premix evenly and homogeneously into feedingstuffsManufacturer
- Manage feed cross-contamination and keep accurate recordsOperator
- Store and use veterinary medicines safely and observe withdrawal periodsFarmer or Animal Keeper
- Fail to comply with specified veterinary medicines dutiesAny Person
186 other provisions — procedural and definitional
Help complying
Guvnor’s practical routes through this instrument.
2 more guides that reference this instrument
Duty extraction and severity labels are Guvnor’s analysis of the instrument, not the instrument itself. Always verify against the linked source text.