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Commission Implementing Decision of 12 November 2013 on the monitoring and reporting of antimicrobial resistance in zoonotic and commensal bacteria (notified under document C(2013) 7145) (Text with EEA relevance) (2013/652/EU)
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5.Quality control and storage of the isolatesU.K.
The laboratories designated by the competent authority to perform the antimicrobial susceptibility testing of the isolates included in the F1... monitoring programme, shall be involved in a quality assurance system including proficiency test set up [F2at national level], in identification, typing and susceptibility testing of the bacteria targeted by the F1... monitoring of AMR.
Textual Amendments
F1Word in Annex Pt. A point 5 omitted (31.12.2020) by virtue of The Zoonotic Disease Eradication and Control (Amendment) (EU Exit) Regulations 2019 (S.I. 2019/740), regs. 1, 11(18)(a); 2020 c. 1, Sch. 5 para. 1(1)
F2Words in Annex Pt. A point 5 substituted (31.12.2020) by The Zoonotic Disease Eradication and Control (Amendment) (EU Exit) Regulations 2019 (S.I. 2019/740), regs. 1, 11(18)(b); 2020 c. 1, Sch. 5 para. 1(1)
Isolates shall be stored by the national reference laboratories for AMR at a temperature of – 80 °C for a minimum period of five years. Other methods of storage may alternatively be used provided that they ensure viability and absence of changes in strain properties.
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