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Autor:
Johanna Andersson, Hans Kjer, Solveig Linko, Britt-Marie Ödlund, Yvonne Couchér, Emil Völkert
Publikováno v:
Accreditation and Quality Assurance. 9:47-51
The European Commission (EC) Directive on in vitro diagnostic medical devices requires—amongst other obligations—manufacturers to establish metrological traceability of values assigned to calibrators to available measurement procedures and/or ava