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the printed package leaflet of the medicinal product must state the name and address of the manufacturer responsible for the release of the concerned batch.
in der druckversion der packungsbeilage des arzneimittels müssen name und anschrift des herstellers, der für die freigabe der betreffenden charge verantwortlich ist, angegeben werden.
dom af 17. april 2013 i sag t-404/11, turbo compressor manufacturer (tcmfg)/rådet for den europæiske union.
urteil des gerichts vom 17. april 2013, rechtssache t-404/11, turbo compressor manufacturer (tcmfg)/rat der europäischen union.