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Sommarju ta' deċiżjonijiet tal-Unjoni Ewropea dwar l-awtorizzazzjonijiet għat-tqegħid fis-suq tal-prodotti mediċinali minn 1 Marzu 2010 sa 30 Gunju 2010 [Deċiżjonijiet meħuda skont l-Artikolu 34 tad-Direttiva 2001/83/KE jew l-Artikolu 38 tad-Direttiva 2001/82/KE]
Sommarju ta' deċiżjonijiet tal-Unjoni Ewropea dwar l-awtorizzazzjonijiet għat-tqegħid fis-suq tal-prodotti mediċinali minn 1 Marzu 2010 sa 30 Gunju 2010 [Deċiżjonijiet meħuda skont l-Artikolu 34 tad-Direttiva 2001/83/KE jew l-Artikolu 38 tad-Direttiva 2001/82/KE]
Publication metadata
- Published:
- Corporate author(s): European Commission
- Subject: EU Member State , market approval , marketing standard , medicinal product , pharmaceutical legislation
- CELEX : 52010XC0924(04)
- OJ : JOC_2010_258_R_0032_01
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