Commission Implementing Decision
of 2 December 2013
authorising a laboratory in the United States of America to carry out serological tests to monitor the effectiveness of rabies vaccines
(notified under document C(2013) 8365)
(Text with EEA relevance)
(2013/709/EU)
THE EUROPEAN COMMISSION,
Having regard to the Treaty on the Functioning of the European Union,
Whereas:
Decision 2000/258/EC designates the Agence française de sécurité sanitaire des aliments (AFSSA) in Nancy, France (integrated since 1 July 2010 into the Agence nationale de sécurité sanitaire de l’alimentation, de l’environnement et du travail, ANSES), as the specific institute responsible for establishing the criteria necessary for standardising the serological tests to monitor the effectiveness of rabies vaccines.
That Decision provides that the ANSES is to document the appraisal of laboratories in third countries that have applied to carry out serological tests to monitor the effectiveness of rabies vaccines.
The competent authority of the United States of America has submitted an application for re-approval of the VETCOM Food Analysis and Diagnostic Laboratory, in Fort Sam Houston which is supported by a favourable appraisal report established for that laboratory by the ANSES dated 16 September 2013.
The competent authority of the United States of America has also officially informed the Commission that the name of the laboratory has changed.
That laboratory should therefore be authorised to carry out serological tests to monitor the effectiveness of rabies vaccines in dogs, cats and ferrets.
The measures provided for in this Decision are in accordance with the opinion of the Standing Committee on the Food Chain and Animal Health,
HAS ADOPTED THIS DECISION: