It was with regret that I learned of the illness due to variant CJD of the young man and I wish to convey my sympathy to his family and friends.
The Minister for Health and Children has dealt with the public health dimension arising from this case. Ireland has operated a range of controls in the cattle and beef sectors against BSE since the confirmation of the first case in 1989. The objective of these controls, which are kept under constant review and are in line with best available scientific knowledge, is to eliminate the cause of the disease and to protect the consumer of Irish beef. The controls were substantially extended in 1997 when a possible link between BSE and variant CJD was first confirmed in the UK. While the EU further extended the mandatory controls on meat and bonemeal and specified risk material removal in late 2000, Ireland put in place the main elements of these in 1996 and 1997 for public health protection.
My Department operates the controls in place in Ireland in the export plants. In small local abattoirs, the local authorities operate the controls under the supervision of the Food Safety Authority of Ireland. Irish BSE controls remain subject to ongoing external audit and examination by a range of bodies, including the Food Safety Authority of Ireland and the European Commission Food and Veterinary Office. Based on an extensive examination in 1998 the EU categorised Ireland's position on BSE controls as optimally stable, which is the highest category of control effectiveness. The Irish BSE control system is also subject to examination by the veterinary and public health authorities in certain non-EU beef importing countries.
In respect of the current case, both the CJD advisory group and the Food Safety Authority of Ireland have indicated that there is no need for concern about the public health and or safety of Irish beef. In particular, the Food Safety Authority of Ireland stated that it is "confident that based on current controls consumers of Irish beef are not being exposed to the BSE infective agent". Animal products from the non-EU countries may be imported only from countries that the EU has approved on the basis that their veterinary, animal health and residue controls for the products in question are at least equivalent to those of member states. Therefore, harmonised provisions are operated in accordance with community legislation and these standards are audited by the EU food and veterinary office. Where there are concerns with regard to the effectiveness of controls being operated in an approved third country, the European Commission, in consultation with the standing committee on the food chain and animal health, may introduce specific controls by means of a safeguard measure to ensure the protection of human and animal health.