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Regolament (KE) Nru 1394/2007 tal-Parlament Ewropew u tal-Kunsill tat- 13 ta’ Novembru 2007 dwar prodotti mediċinali ta’ terapija avvanzata u li jemenda d-Direttiva 2001/83/KE u r-Regolament (KE) Nru 726/2004 (Test b’rilevanza għaż-ŻEE)
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