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Regolament (UE) Nru 536/2014 tal-Parlament Ewropew u tal-Kunsill tas- 16 ta' April 2014 dwar il-provi kliniċi fuq prodotti mediċinali għall-użu mill-bniedem, u li jħassar id-Direttiva 2001/20/KE Test b'rilevanza għaż-ŻEE
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