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Inspections and Investigations Team (IIT) Inspection reports of inspections...
Typed reports and handwritten 'Confirmartion Of Inspection Reports' issued to a business after an inspection has taken place. -
Pharmacovigilance data about most commonly reported adverse reactions and...
Datasets providing information about the most commonly reported adverse reaction events and suspect lack of efficacy for difference classes of veterinary medicines. -
Special Import/Special Treatment Certificates for imported use of veterinary...
These certificates are produced and released to the applicant upon approval of an application to import a medicine from outside the UK. -
Veterinary Medicines Regulations (VMR) - consultation data
List of consultees for consultation exercises on the Veterinary Medicines Regulations (VMR) and related consultations. -
Reports from the EU Committee of Veterinary Medicinal Products meetings (24...
Veterinary Medicines Directorate (VMD) internal report of the EU Committee of Veterinary Medicinal Products meeting -
Inspections and Investigations Team (IIT) Investigations notes of...
Details of investigations, including the source of information, the investigation procedure and the outcome, held on the Inspections Management System (IMS) database. -
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)). -
Inspections and Investigations (IIT) team inspection notes of inspections of...
Inspectors' inspection notes held on the Inspections Management System (IMS) database. -
Good Manufacturing Practice Inspections Team (GMPIT) inspections of...
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...
Results of proportinal reporting ration analyses and investigations into the signals detected. -
Spontaneous adverse event reports following bad reactions to or lack of...
Individual case summaries of animals or humans reacting to veterinary medicines -
Questions from companies seeking Marketing Authorisations for veterinary...
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... -
Periodic Safety Update Reports from Marketing Authorisation holders about...
Documents submitted by companies as part of their regulatory obligations, summarising all adverse events reported in a predefined period.