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VMDB

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uuid00smxpv

Namestring
VMDB
Legal namestring
Veterinary Medicines Directorate
Company typeenum
Private
Founded yearstring
-
Descriptiontext

The Veterinary Medicines Directorate (VMDB) is a UK government executive agency, sponsored by the Department for Environment, Food & Rural Affairs (DEFRA), responsible for the regulatory oversight of veterinary medicines in the United Kingdom. Its mandate covers pre-market assessment and authorisation of veterinary biologics and animal vaccines, pharmacovigilance monitoring, adverse event reporting, and publication of public registers for manufacturing and distribution. The agency is headquartered in Addlestone, Surrey, and serves Marketing Authorisation Holders in the animal medicines industry as its primary regulated constituency, with downstream constituencies of farmers, pet owners, and food supply chain stakeholders.

VMDB operates a portfolio of digital services delivered through the GOV.UK platform rather than a commercial product suite. Core products include the Product Information Database (a public lookup for licensed animal medicines), the Veterinary Medicines Digital Service (a pharmacovigilance submission portal for Marketing Authorisation Holders), the VMD Information Hub (a centralised guidance and regulatory resource), the Adverse Event Reporting Portal, the Veterinary Medicines Registers for manufacturers and distributors, and the Veterinary Medicines Guidance Notes (VMGNs). New digital services — including the Adverse Event Reporting Portal, the Online Contact Form, and the Veterinary Medicines Digital Service — were launched in May–July 2026 as part of an ongoing digitisation programme.

VMDB does not operate on a commercial revenue model. It is funded through UK government appropriations and regulatory fees, has no private shareholders, and reports publicly through DEFRA-aligned annual report and accounts. Its strategic posture is increasingly outward-facing, evidenced by a December 2025 Memorandum of Understanding with the Canadian Food Inspection Agency (CFIA) covering joint reviews of veterinary biologics. Leadership comprises CEO Abigail Seager, Deputy CEO/Director of Authorisations Gavin Hall, and non-executive directors Alison White, Laura Catterick, Mike Venables OBE, and David Catlow.

Short descriptiontext

VMDB is a UK government executive agency, sponsored by DEFRA, that regulates veterinary medicines in the United Kingdom. It authorises products, monitors pharmacovigilance, and operates digital services for Marketing Authorisation Holders, farmers, pet owners, and food supply stakeholders.

Operating statusenum
Operating
Ownership categoryenum
akta.pro rankint
HeadquartersAddlestone, United Kingdom
HQ citystring
Addlestone
HQ countrystring
United Kingdom
HQ regionstring
Europe
Markets served

Serves global market

Offices1 record

Each record includes

City, Country, Type, Description, Source

Keyword5 values
veterinary medicines regulation, animal health oversight, pharmacovigilance reporting, marketing authorisation, adverse event monitoring
Industry2 codes
1Veterinary Regulatory Authorities (Licensing, Compliance & Enforcement)
CodeHLAMAJACPrimaryYes
2Vaccine Pharmacovigilance & Post-Market Surveillance
CodeHLAMAKANPrimaryNo
Product category
Veterinary Medicines Regulation
Marketing channels6 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels4 records

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components5 values
Personnel, Operations, Technology or R&D, Infrastructure, Others
GTM typeB2B
B2B
Offering typeServices
Services
Core offering1 text field

The Veterinary Medicines Directorate (VMDB) is a UK government executive agency that provides statutory regulatory oversight of veterinary medicines in the UK. It assesses and authorises animal medicines, monitors adverse events, maintains public registers of licensed products, manufacturers and distributors, and offers digital services for Marketing Authorisation Holders to submit pharmacovigilance reports and manage regulatory compliance. Its mission is to protect animal health, public health and the environment by ensuring veterinary medicines meet safety, efficacy and quality standards.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 2 values shown
  • Reduced duplication in regulatory reviews through joint review mechanisms
+1 more record
Product overview1 text field

The Veterinary Medicines Directorate (VMDB) is a UK government regulatory agency that operates a portfolio of digital services and informational products rather than a commercial product suite. The core offerings include the Product Information Database for verifying licensed animal medicines, the Veterinary Medicines Digital Service for pharmacovigilance reporting by Marketing Authorisation Holders, the VMD Information Hub for regulatory guidance, and an Online Contact Form for general enquiries. These digital services are complemented by guidance documentation (VMGNs) and public registers for manufacturing and distribution transparency. VMDB functions as an executive agency sponsored by the Department for Environment, Food & Rural Affairs (DEFRA), focused on protecting animal health, public health, and the environment through regulatory oversight.

Product and service7 records
1Product Information Database
CategoryRegulatory information service
Description

Public database service that allows users to check whether an animal medicine is licensed in the UK. It is targeted at pet owners, farmers, veterinarians and the animal medicines industry needing to verify the authorised status of veterinary products.

2Veterinary Medicines Digital Service
CategoryRegulatory digital service
Description

Digital service platform enabling Marketing Authorisation Holders to submit pharmacovigilance reports and manage regulatory compliance workflows with the UK veterinary medicines regulator.

3VMD Information Hub
CategoryRegulatory information service
Description

Centralised online hub providing regulatory guidance, regulations and resources related to veterinary medicines in the UK for Marketing Authorisation Holders, veterinarians and the public.

4Online Contact Form
CategoryRegulatory digital service
Description

Digital service for general enquiries and contacting the VMD, serving as the main route for communications with the agency.

5Adverse Event Reporting Portal
CategoryRegulatory digital service
Description

Digital service for reporting problems with animal medicines or animals exposed to human medicine, enabling easier and more efficient adverse event reporting.

6Veterinary Medicines Registers
CategoryRegulatory information service
Description

Public registers for manufacturing and distribution of veterinary medicines, providing transparency on authorised manufacturers and distributors operating in the UK.

7Veterinary Medicines Guidance Notes (VMGNs)
CategoryRegulatory guidance
Description

Detailed guidance documentation on the regulations and rules governing veterinary medicines in the UK, used by industry applicants and regulators.

Scale indicator2 records

Each record includes

Type, Value, Description, Source

Partnership2 partners
1Canadian Food Inspection Agency (CFIA)
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2025-12-17
Description

Official Memorandum of Understanding signed between VMD and CFIA to enhance collaboration on regulatory oversight of veterinary biologics, including animal vaccines. The agreement aims to make pre-market assessment and approval more efficient by sharing scientific expertise, discussing common priorities, and exploring joint reviews to reduce duplication and facilitate access to products.

newswire.ca
2Department for Environment, Food & Rural Affairs (DEFRA)
Strategic tierCoreTypeOthers
Description

VMD is an executive agency sponsored by DEFRA. DEFRA is the parent government department providing strategic oversight and policy direction for the Veterinary Medicines Directorate.

gov.uk
Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight4 records

Each record includes

Type, Description

Peers10 records
1European Medicines Agency (EMA)
TypeBroad incumbent
Description

EU-level regulator for human and veterinary medicines. EMA is comparable to VMD because both authorize and oversee veterinary medicinal products, though EMA operates across EU member states rather than just the UK.

2U.S. Food and Drug Administration - Center for Veterinary Medicine (FDA-CVM)
TypeBroad incumbent
Description

U.S. federal regulator for veterinary drugs and medicated feeds. FDA-CVM performs the same statutory authorization, pharmacovigilance, and adverse event oversight functions as VMD, but at US national scale.

3Health Canada - Veterinary Drugs Directorate (VDD)
TypeDirect peer
Description

Canadian national authority for veterinary drug approval and oversight. VDD is VMD's most direct peer because both regulate veterinary pharmaceuticals/biologics at the national level and the agencies have an active MOU on biologics collaboration.

4Canadian Food Inspection Agency (CFIA)
TypeDirect peer
Description

Canadian regulator for veterinary biologics including animal vaccines. CFIA is a direct peer and counterparty to VMD under their December 2025 MOU on biologics oversight, with overlapping scope in vaccine authorization.

5Australian Pesticides and Veterinary Medicines Authority (APVMA)
TypeBroad incumbent
Description

Australian regulator for agricultural chemicals and veterinary medicines. APVMA is comparable as a national veterinary medicines regulator handling product authorisation and adverse event reporting.

6Health Products Regulatory Authority (HPRA) - Ireland
TypeRegional player
Description

Irish regulator for human and veterinary medicines. HPRA shares historical ties to the UK regulatory framework pre-Brexit and continues to perform similar veterinary drug oversight for the Irish market.

7Federal Office of Consumer Protection and Food Safety (BVL) - Germany
TypeRegional player
Description

German federal authority for veterinary medicinal product authorization and pharmacovigilance. BVL performs VMD-equivalent functions at the national level within the EU regulatory network.

8Medicines and Healthcare products Regulatory Agency (MHRA)
TypeBroad incumbent
Description

UK regulator for human medicines and medical devices. MHRA is a peer UK executive agency under the same government ecosystem as VMD, sharing GOV.UK digital infrastructure and DEFRA-adjacent governance models.

9Spanish Agency of Medicines and Medical Devices (AEMPS)
TypeRegional player
Description

Spanish national regulator for human and veterinary medicines. AEMPS performs VMD-equivalent veterinary authorisation and pharmacovigilance functions within the EU regulatory network.

10Swissmedic
TypeRegional player
Description

Swiss national authority for human and veterinary medicines. Swissmedic conducts VMD-comparable authorization and post-market surveillance for veterinary medicinal products in a non-EU jurisdiction.

Market position
Strengths4 records

Each record includes

Headline, Details, Source

Weaknesses4 records

Each record includes

Headline, Details, Source

Competitive moat4 records

Each record includes

Type, Details

Key risks5 records

Each record includes

Headline, Details, Source

Key highlights6 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Segment3 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile3 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
No
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature3 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles6 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

No data
No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

VMDB

Veterinary Medicines Regulationvmd.defra.gov.uk

VMDB is a UK government executive agency, sponsored by DEFRA, that regulates veterinary medicines in the United Kingdom. It authorises products, monitors pharmacovigilance, and operates digital services for Marketing Authorisation Holders, farmers, pet owners, and food supply stakeholders.

What VMDB does

The Veterinary Medicines Directorate (VMDB) is a UK government executive agency, sponsored by the Department for Environment, Food & Rural Affairs (DEFRA), responsible for the regulatory oversight of veterinary medicines in the United Kingdom. Its mandate covers pre-market assessment and authorisation of veterinary biologics and animal vaccines, pharmacovigilance monitoring, adverse event reporting, and publication of public registers for manufacturing and distribution. The agency is headquartered in Addlestone, Surrey, and serves Marketing Authorisation Holders in the animal medicines industry as its primary regulated constituency, with downstream constituencies of farmers, pet owners, and food supply chain stakeholders.

VMDB operates a portfolio of digital services delivered through the GOV.UK platform rather than a commercial product suite. Core products include the Product Information Database (a public lookup for licensed animal medicines), the Veterinary Medicines Digital Service (a pharmacovigilance submission portal for Marketing Authorisation Holders), the VMD Information Hub (a centralised guidance and regulatory resource), the Adverse Event Reporting Portal, the Veterinary Medicines Registers for manufacturers and distributors, and the Veterinary Medicines Guidance Notes (VMGNs). New digital services — including the Adverse Event Reporting Portal, the Online Contact Form, and the Veterinary Medicines Digital Service — were launched in May–July 2026 as part of an ongoing digitisation programme.

VMDB does not operate on a commercial revenue model. It is funded through UK government appropriations and regulatory fees, has no private shareholders, and reports publicly through DEFRA-aligned annual report and accounts. Its strategic posture is increasingly outward-facing, evidenced by a December 2025 Memorandum of Understanding with the Canadian Food Inspection Agency (CFIA) covering joint reviews of veterinary biologics. Leadership comprises CEO Abigail Seager, Deputy CEO/Director of Authorisations Gavin Hall, and non-executive directors Alison White, Laura Catterick, Mike Venables OBE, and David Catlow.

VMDB firmographics

Firmographics
Name
VMDB
Legal name
Veterinary Medicines Directorate
Website
https://vmd.defra.gov.uk
Company type
Private
Operating status
Operating
Short description
VMDB is a UK government executive agency, sponsored by DEFRA, that regulates veterinary medicines in the United Kingdom. It authorises products, monitors pharmacovigilance, and operates digital services for Marketing Authorisation Holders, farmers, pet owners, and food supply stakeholders.
Ownership category
akta.pro rank

VMDB industry classification

Industry
Product category
Veterinary Medicines Regulation
akta.pro primary industry
Veterinary Regulatory Authorities (Licensing, Compliance & Enforcement) (HLAMAJAC)
akta.pro secondary industry
Vaccine Pharmacovigilance & Post-Market Surveillance (HLAMAKAN)

Keywords

  • Veterinary medicines regulation
  • Animal health oversight
  • Pharmacovigilance reporting
  • Marketing authorisation
  • Adverse event monitoring

Where VMDB is headquartered

Location

Headquarters

HQ city
Addlestone
HQ country
United Kingdom
HQ region
Europe

Offices1 record

Markets served

VMDB business model

Business model
GTM type
B2B
Offering type
Services
Cost components
Personnel, Operations, Technology or R&D, Infrastructure, Others

Distribution channels4 records

Marketing channels6 records

VMDB product offering

Product offering

Core offering

The Veterinary Medicines Directorate (VMDB) is a UK government executive agency that provides statutory regulatory oversight of veterinary medicines in the UK. It assesses and authorises animal medicines, monitors adverse events, maintains public registers of licensed products, manufacturers and distributors, and offers digital services for Marketing Authorisation Holders to submit pharmacovigilance reports and manage regulatory compliance. Its mission is to protect animal health, public health and the environment by ensuring veterinary medicines meet safety, efficacy and quality standards.

Product overview

The Veterinary Medicines Directorate (VMDB) is a UK government regulatory agency that operates a portfolio of digital services and informational products rather than a commercial product suite. The core offerings include the Product Information Database for verifying licensed animal medicines, the Veterinary Medicines Digital Service for pharmacovigilance reporting by Marketing Authorisation Holders, the VMD Information Hub for regulatory guidance, and an Online Contact Form for general enquiries. These digital services are complemented by guidance documentation (VMGNs) and public registers for manufacturing and distribution transparency. VMDB functions as an executive agency sponsored by the Department for Environment, Food & Rural Affairs (DEFRA), focused on protecting animal health, public health, and the environment through regulatory oversight.

Differentiator

Problem solved

Functional benefit

Products and services

  • Product Information Database Public database service that allows users to check whether an animal medicine is licensed in the UK. It is targeted at pet owners, farmers, veterinarians and the animal medicines industry needing to verify the authorised status of veterinary products.
  • Veterinary Medicines Digital Service Digital service platform enabling Marketing Authorisation Holders to submit pharmacovigilance reports and manage regulatory compliance workflows with the UK veterinary medicines regulator.
  • VMD Information Hub Centralised online hub providing regulatory guidance, regulations and resources related to veterinary medicines in the UK for Marketing Authorisation Holders, veterinarians and the public.
  • Online Contact Form Digital service for general enquiries and contacting the VMD, serving as the main route for communications with the agency.
  • Adverse Event Reporting Portal Digital service for reporting problems with animal medicines or animals exposed to human medicine, enabling easier and more efficient adverse event reporting.
  • Veterinary Medicines Registers Public registers for manufacturing and distribution of veterinary medicines, providing transparency on authorised manufacturers and distributors operating in the UK.
  • Veterinary Medicines Guidance Notes (VMGNs) Detailed guidance documentation on the regulations and rules governing veterinary medicines in the UK, used by industry applicants and regulators.

Quantifiable outcome

  • Reduced duplication in regulatory reviews through joint review mechanisms
  • +1 more outcomes

Companies that use VMDB

Customer profile

Segments3 records

Ideal customer profiles3 records

VMDB technology and API

Technology

Technology focussed No

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature3 records

VMDB partnerships and signals

Strategic signal

Partnerships

Two partnerships are on record, tiered core.

  • Canadian Food Inspection Agency (CFIA)coreStrategic or Co-development Partner · 17 December 2025Official Memorandum of Understanding signed between VMD and CFIA to enhance collaboration on regulatory oversight of veterinary biologics, including animal vaccines. The agreement aims to make pre-market assessment and approval more efficient by sharing scientific expertise, discussing common priorities, and exploring joint reviews to reduce duplication and facilitate access to products.
  • Department for Environment, Food & Rural Affairs (DEFRA)coreOthersVMD is an executive agency sponsored by DEFRA. DEFRA is the parent government department providing strategic oversight and policy direction for the Veterinary Medicines Directorate.

Scale indicators2 records

Recent moves6 records

Expansion highlights4 records

VMDB competitors and assessment

Company assessment

Broad incumbents

  • European Medicines Agency (EMA): EU-level regulator for human and veterinary medicines. EMA is comparable to VMD because both authorize and oversee veterinary medicinal products, though EMA operates across EU member states rather than just the UK.
  • U.S. Food and Drug Administration - Center for Veterinary Medicine (FDA-CVM): U.S. federal regulator for veterinary drugs and medicated feeds. FDA-CVM performs the same statutory authorization, pharmacovigilance, and adverse event oversight functions as VMD, but at US national scale.
  • Australian Pesticides and Veterinary Medicines Authority (APVMA): Australian regulator for agricultural chemicals and veterinary medicines. APVMA is comparable as a national veterinary medicines regulator handling product authorisation and adverse event reporting.
  • Medicines and Healthcare products Regulatory Agency (MHRA): UK regulator for human medicines and medical devices. MHRA is a peer UK executive agency under the same government ecosystem as VMD, sharing GOV.UK digital infrastructure and DEFRA-adjacent governance models.

Direct peers

  • Health Canada - Veterinary Drugs Directorate (VDD): Canadian national authority for veterinary drug approval and oversight. VDD is VMD's most direct peer because both regulate veterinary pharmaceuticals/biologics at the national level and the agencies have an active MOU on biologics collaboration.
  • Canadian Food Inspection Agency (CFIA): Canadian regulator for veterinary biologics including animal vaccines. CFIA is a direct peer and counterparty to VMD under their December 2025 MOU on biologics oversight, with overlapping scope in vaccine authorization.

Regional players

  • Health Products Regulatory Authority (HPRA) - Ireland: Irish regulator for human and veterinary medicines. HPRA shares historical ties to the UK regulatory framework pre-Brexit and continues to perform similar veterinary drug oversight for the Irish market.
  • Federal Office of Consumer Protection and Food Safety (BVL) - Germany: German federal authority for veterinary medicinal product authorization and pharmacovigilance. BVL performs VMD-equivalent functions at the national level within the EU regulatory network.
  • Spanish Agency of Medicines and Medical Devices (AEMPS): Spanish national regulator for human and veterinary medicines. AEMPS performs VMD-equivalent veterinary authorisation and pharmacovigilance functions within the EU regulatory network.
  • Swissmedic: Swiss national authority for human and veterinary medicines. Swissmedic conducts VMD-comparable authorization and post-market surveillance for veterinary medicinal products in a non-EU jurisdiction.

Market position

Strengths4 records

Weaknesses4 records

Competitive moat4 records

Key risks5 records

Key highlights6 records

Customer concentration

VMDB social profiles

Digital presence

VMDB financial estimates

Financial estimate

Revenue estimate

Valuation estimate

VMDB leadership team

Management profile

Number of profiles

Profiles6 records

VMDB funding detail

Funding detail

Funding overview

Funding rounds

Investors

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

VMDB M&A and investment

M&A and investment

M&A

Investments

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about VMDB

What does VMDB do?

The Veterinary Medicines Directorate (VMDB) is a UK government executive agency that provides statutory regulatory oversight of veterinary medicines in the UK. It assesses and authorises animal medicines, monitors adverse events, maintains public registers of licensed products, manufacturers and distributors, and offers digital services for Marketing Authorisation Holders to submit pharmacovigilance reports and manage regulatory compliance. Its mission is to protect animal health, public health and the environment by ensuring veterinary medicines meet safety, efficacy and quality standards.

Is VMDB a public or private company?

VMDB is a private company. It is classified as state government owned and is currently operating.

When was VMDB founded?

VMDB was founded in -1.

Where is VMDB based?

VMDB is headquartered in Addlestone, United Kingdom, in the Europe region.

Who are VMDB's main competitors?

Broad incumbents on record are European Medicines Agency (EMA), U.S. Food and Drug Administration - Center for Veterinary Medicine (FDA-CVM), Australian Pesticides and Veterinary Medicines Authority (APVMA) and Medicines and Healthcare products Regulatory Agency (MHRA). Direct peers are Health Canada - Veterinary Drugs Directorate (VDD) and Canadian Food Inspection Agency (CFIA). Regional players are Health Products Regulatory Authority (HPRA) - Ireland, Federal Office of Consumer Protection and Food Safety (BVL) - Germany, Spanish Agency of Medicines and Medical Devices (AEMPS) and Swissmedic.

Does VMDB have an API?

No public API is recorded for VMDB.

What industry is VMDB in?

VMDB's product category is Veterinary Medicines Regulation. Its primary akta.pro industry code is HLAMAJAC, Veterinary Regulatory Authorities (Licensing, Compliance & Enforcement), with a secondary code of HLAMAKAN, Vaccine Pharmacovigilance & Post-Market Surveillance.

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Live signals
UK GovernmentAnimal use in veterinary vaccines quality control falls to lowest levels in a decadeThe UK's Veterinary Medicines Directorate reported that the average number of animals needed to release a batch of veterinary vaccine fell by 41% from 29 in 2013 to 17 in 2024. Overall animal use dropped 29% despite more vaccines being released, driven by science advances and alternative testing. The report notes animal testing remains challenging for some vaccines like clostridial and fish vaccines.UK GovernmentPharmacovigilance Senior Assessor and Reporting LeadThe Veterinary Medicines Directorate is hiring a Pharmacovigilance Senior Assessor and Reporting Lead for post-authorisation surveillance of veterinary medicines in the UK. The G7 role offers a salary of £64,015 per annum with pension and 25 days' annual leave, with applications due 12 October 2026.Open Access GovernmentLivestock keepers urged to be consider vaccination as bluetongue cases riseThe UK Chief Veterinary Officer has urged livestock keepers across Great Britain to consider immediate vaccination as bluetongue virus cases rise due to favorable weather conditions for midges. The Department for Environment, Food & Rural Affairs and the Veterinary Medicines Directorate are coordinating with manufacturers to secure additional vaccine stocks to meet rising demand. Regulatory measures include movement restrictions in England and Wales, while the Animal and Plant Health Agency handles reporting and the Pirbright Institute conducts diagnostic testing.Mirage NewsCommunications Officer Recruitment LaunchedThe Veterinary Medicines Directorate (VMD) has launched a recruitment process for a Communications Officer position at Grade AO. The role involves managing external enquiries, coordinating internal communications such as staff newsletters, and publishing content on GOV.UK in accordance with accessibility guidelines. Applications are to be submitted via the Civil Service Jobs portal by the closing date of 31 August 2026.UK GovernmentMaprelin 75 µg/ml Solution for Injection for Pigs - Product defect recallAnupco Ltd T/A Kela Animal Health UK has initiated a Class II recall for Maprelin 75 µg/ml Solution for Injection for Pigs due to an increased risk of microbial contamination in products manufactured between January and May 2025. The Veterinary Medicines Directorate published this notice on October 14, 2025, requiring wholesalers to quarantine specific batches with expiry dates in 2026.NewswireCanada and the United Kingdom agree to work together to improve regulatory efficiency for animal vaccinesThe Canadian Food Inspection Agency (CFIA) and the UK's Veterinary Medicines Directorate (VMD) have officially signed a Memorandum of Understanding to enhance collaboration on regulatory oversight of veterinary biologics, including animal vaccines. The agreement aims to make pre-market assessment and approval more efficient by sharing scientific expertise, discussing common priorities, and exploring joint reviews to reduce duplication and facilitate access to products. This MOU is designed to protect animal health, support farmers and pet owners, and safeguard the food supply chain.UK GovernmentBatch recall Anesketin 100 mg/ml Solution for Injection for Dogs, Cats and HorsesDechra Pharmaceuticals PLC initiated a Class II recall for specific batches of Anesketin 100 mg/ml Solution for Injection used in dogs, cats, and horses due to the presence of visible particles in the vials. The Veterinary Medicines Directorate published this alert on 28 November 2025, instructing veterinarians and wholesalers to quarantine the affected inventory immediately.Farmers GuideLatest RUMA Agriculture Targets Task Force report releasedThe RUMA Agriculture Targets Task Force released its final TTF2 report, confirming continued progress in antibiotic stewardship within the UK livestock industry ahead of the third cycle's launch. The report indicates that while overall antibiotic use remains low, some sectors saw increased usage due to disease outbreaks, highlighting the need for responsible access to medicines. This release coincides with the Veterinary Medicines Directorate’s VARSS report, which reinforces the link between reduced antibiotic use and lower antimicrobial resistance.The GuardianTake the bull by the hornsThe author argues that the foot and mouth disease outbreak exposed how the UK's veterinary medicines and pesticides directorates remain unreformed, still housed within Defra rather than the Food Standards Agency. It notes the Veterinary Medicines Directorate's advisory committees are exempt from FSA transparency rules and are funded by drug companies, with many members holding commercial interests.