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The Veterinary Medicine Directorate's Research and Development programme

Project proposals, peer review reports and interim reports

Veterinary Medicines Regulations (VMR) - enforcement data

Data on individual enforcement cases (e.g. Intelligence, information supplied/gatherered about possible breaches of the Veterinary Medicines Regulations (VMR)).

Periodic Safety Update Reports from Marketing Authorisation holders about pharmacovigilance data on their products

Documents submitted by companies as part of their regulatory obligations, summarising all adverse events reported in a predefined period.

Inspections and Investigations (IIT) team inspection notes of inspections of approved businesses and registered Veterinary Practice Premises

Inspectors' inspection notes held on the Inspections Management System (IMS) database.

Good Manufacturing Practice Inspections Team (GMPIT) inspections of manufacturing premises of veterinary medicines

Material relating to Veterinary Medicines Directorate VMD inspections (e.g. Inspection reports, agendas, notes). The VMD's own internal inspection schedule.

Documents relating to the VMD's internal Alert Group which considers significance of pharmacovigilance data received on veterinary medicinal products

Results of proportinal reporting ration analyses and investigations into the signals detected.

Antimicrobial Resistance surveillance data

Antimicrobial Resistance (AMR) data gives the results of antimicrobial sensitivity testing on Salmonella isolates from samples collected from poultry and other animal species under the statutory...

Spontaneous adverse event reports following bad reactions to or lack of effectiveness of veterinary medicines

Individual case summaries of animals or humans reacting to veterinary medicines

Questions from companies seeking Marketing Authorisations for veterinary medicinal products as part of the assessment process

The General Assessment Team routinely receive queries from companies in relation to Marketing Authorisations. A summary Q&A document is on the VMD website to address generic frequently asked...

Residues Surveillance

Details of samples taken under the Residues Surveillance Programme in GB.

Good Manufacturing Practice (GMP) & Good Distribution Practice (GDP) Inspections

The data provides information on Good Manufacturing Practice (GMP) inspections of manufacturers of veterinary medicines; and Good Distribution Practice (GDP) inspections of veterinary wholesale...

Batch release of immunological veterinary medicinal products

batches of immunological product released under Articles 81a and 81b of EU Directive 2001/82/EC, as amended

Veterinary Medicines Directorate (VMD) Organogram

Staff in post at the VMD

Clinical signs listed in Periodic Safety Update report data submitted to the VMD

The dataset includes all the clinical signs included in the line listings submitted with periodic safety update reports submitted to the Veterinary Medicines Directorate during a one year period....