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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.

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)).

Veterinary Medicines Regulations (VMR) - consultation data

List of consultees for consultation exercises on the Veterinary Medicines Regulations (VMR) and related consultations.

Special Import/Special Treatment Certificates for imported use of veterinary medicines

These certificates are produced and released to the applicant upon approval of an application to import a medicine from outside the UK.

The Veterinary Medicine Directorate's Research and Development programme

Project proposals, peer review reports and interim reports

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.

Imported veterinary medicines

A list of details of the top 10 products for which Special Import Certificates were granted, naming the active ingredient and number of certificates.

Inspections and Investigations Team (IIT) Inspection reports of inspections of approved businesses and registered Veterinary Practice Premises

Typed reports and handwritten 'Confirmartion Of Inspection Reports' issued to a business after an inspection has taken place.

Reports from the EU Committee of Veterinary Medicinal Products meetings (24 hour reports)

Veterinary Medicines Directorate (VMD) internal report of the EU Committee of Veterinary Medicinal Products meeting

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...

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

Details of investigations, including the source of information, the investigation procedure and the outcome, held on the Inspections Management System (IMS) database.

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

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.

Analysis of animal usage in batch release tests

Reports on statistics of animal usage in batch release tests for immunological products