EFSA has asked Member States to provide any information they have on the disease and to share national risk assessments, in particular those countries which have been affected by the disease. EFSA will collect and co-ordinate this information and develop a co-operation network of EU Member State experts and National Agencies involved in risk assessment on Animal health, pooling together all of European and international scientific information on the disease. Depending on the availability and robustness of scientific data, EFSA will invite Member State experts to exchange views with the AHAW Panel’s Working Group on Bluetongue on the available data and develop scientific advice on the containment of Bluetongue in Europe. EFSA will also work in close collaboration with the European Commission, the Community Reference laboratory for Bluetongue and other world reference laboratories.

According to EFSA’s AHAW Panel, in order to develop effective scientific advice and provide technical support to the European Commission and the Member States, it will be necessary to:

• harmonise epidemiological data collection systems and sampling procedures
• develop a method for the quick exchange and sharing of information between Member States
• investigate the origin of the introduction of Bluetongue serotype 8 into the EU

Concerning the introduction of Bluetongue into the EU, the AHAW Panel believes that it is important to have a better understanding of the conditions associated with the spread and possible persistence of the disease and of the role of vector species other than Culicoïdes imicola involved in the spread of infection. It will also be necessary to analyse where and how Culicoides vectors, such as midges, act in the various EU regions and surrounding areas of the EU.