Guidelines
The IMB has published a range of guidance documents that provide information on the regulation of veterinary medicines. These guidelines include advice and direction for companies in relation to product issues, such as authorisations, renewals and variations, as well as adverse reaction reporting and fees.
Up-to-date versions of all veterinary guidelines are available from the publications section of our website.
Forms
When submitting a request to the IMB in relation to the regulatory services we provide, companies should complete the necessary application or notification form. In addition, where necessary, you should also complete the fee application form.
Up-to-date versions of all veterinary forms are available from the publications section of our website.
Pharmacovigilance Forms
To report an adverse reaction resulting from the use of a veterinary medicine, please use one of the following forms.
Further information is available from Adverse Reaction Reporting section of our website.