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Measures to be taken in case of non-compliances related to VMPs and their residues
Regolament Delegat tal-Kummissjoni (UE) 2019/2090 tad-19 ta’ Ġunju 2019 li jissupplimenta r-Regolament (UE) 2017/625 tal-Parlament Ewropew u tal-Kunsill rigward każijiet ta’ nonkonformità suspettata jew stabbilita mar-regoli tal-Unjoni applikabbli għall-użu jew għar-residwi ta’ sustanzi farmakoloġikament attivi awtorizzati fi prodotti mediċinali veterinarji jew bħala addittivi tal-għalf jew mar-regoli tal-Unjoni applikabbli għall-użu jew għar-residwi ta’ sustanzi farmakoloġikament attivi pprojbiti jew mhux awtorizzati (Test b’rilevanza għaż-ŻEE)
The Commission Delegated Regulation specifies the measures to be taken by the competent authorities for specific cases of non-compliance or suspicions of non-compliance of animals and goods from the EU or third countries related to veterinary medicinal products and their residues.