This document describes general workflows and protocols for the validation and the verification of qualitative screening tests for the detection of residues of veterinary drugs in liquid milk (raw, pasteurized, UHT and reconstituted milk powders and whey protein extracts) including biological methods. This guideline does not cover the validation of residue analysis by HPLC, UHPLC or LC MS/MS.
Označení | ČSN P CEN ISO/TS 23758 (570557) |
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Katalogové číslo | 513500 |
Cena | 440 Kč440 |
Datum schválení | 1. 2. 2022 |
Datum účinnosti | 1. 3. 2022 |
Jazyk | angličtina (obsahuje pouze anglický originál) |
Počet stran | 48 stran formátu A4 |
EAN kód | 8596135135004 |
Dostupnost | skladem (tisk na počkání) |