Devices used for the synchronisation of oestrus in bovines are animal remedies that contain hormones and that may be marketed in Ireland and elsewhere in the EU under a specific exception to the EU hormone ban. The relevant EU legislation, however, attaches strict conditions to the availability of these animal remedies. As a result, they are designated as prescription only medicines by the Irish Medicines Board which is the licensing authority for Ireland.
The Animal Remedies Regulations, 1996, which govern, inter alia, how medicines are prescribed, have been in operation for nearly three years. My Department has been engaged in reviewing the operation of the legislation generally, including in relation to this type of animal remedy. In doing so, account is being taken of the various views expressed on the practical impact of the legislation and of the need to ensure that efforts aimed at improving the quality of the national herd are not unduly hampered.
There has been wide-ranging consultation and it is hoped that the review will be completed shortly. I should, however, emphasise that it is not intended to fundamentally alter the thrust of the legislation. Any adjustments must be consistent with the relevant EU legislation and with the maintenance of the highest possible standards of public and animal health protection.