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2013/709/EU: 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: 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

Decision · 3 articles

Data as of 2026-07-04 · Compiled from an official source version. Later amendments or repeals may not be reflected; the official text prevails. · Read the official text ↗

Article 1

In accordance with Article 3(2) of Decision 2000/258/EC, the following laboratory is authorised to perform the serological tests to monitor the effectiveness of rabies vaccines in dogs, cats and ferrets: DoD Food Analysis & Diagnostic Laboratory 2899 Schofield Road JBSA Fort Sam Houston, TX 78234 United States of America

Article 2

This Decision shall apply from 1 January 2014.

Article 3

This Decision is addressed to the Member States.

Source: EUR-Lex (Publications Office of the EU), © European Union, reuse permitted under Commission Decision 2011/833/EU.

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