Regolament ta' Delega tal-Kummissjoni (UE) Nru 1252/2014 tat- 28 ta' Mejju 2014 li jissupplimenta d-Direttiva 2001/83/KE tal-Parlament Ewropew u tal-Kunsill fir-rigward ta' prinċipji u linji gwida ta' prassi tajba ta' manifattura għas-sustanzi attivi għal prodotti mediċinali għall-użu mill-bniedem Test b'rilevanza għaż-ŻEE

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