The evolution of the regulatory framework for the plasma and plasma-derived medicinal products system in Italy
- PMID: 24333315
- PMCID: PMC3853985
- DOI: 10.2450/2013.003s
The evolution of the regulatory framework for the plasma and plasma-derived medicinal products system in Italy
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References
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- European Directorate for the Quality of Medicine & Health Care, Council of Europe. Guide to the Preparation, Use and Quality Assurance of Blood Components. Recommendation No. R (95) 15. 17th Edition. Strasbourg, France: 2013. (2013)
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- Official Journal of Italian Republic no. 147 June 26th, 2012. Decreto del Ministro della Salute 12 aprile 2012 recante “Schema tipo di convenzione tra le Regioni e le Province autonome e le Aziende produttrici di medicinali emoderivati per la lavorazione del plasma raccolto sul territorio nazionale”. [Accessed on 30/08/2013]. Available at: http://www.centronazionalesangue.it/sites/default/files/dd.mm_._12.04.20....
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- Official Journal of Italian Republic no. 147 June 26th, 2012. Decreto del Ministro della Salute 12 aprile 2012 “Modalità per la presentazione e valutazione delle istanze volte ad ottenere l’inserimento tra i centri e le aziende di produzione di medicinali emoderivati autorizzati alla stipula delle convenzioni con le Regioni e le Province Autonome per la lavorazione del plasma raccolto sul territorio nazionale”. [Accessed on 30/08/2013]. Available at: http://www.centronazionalesangue.it/sites/default/files/dd.mm_._12.04.20....
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- Official Journal of Italian Republic no. 147 June 26th, 2012. Decreto del Ministro della Salute 12 aprile 2012 “Disposizioni sull’importazione ed esportazione del sangue umano e dei suoi prodotti”. [Accessed on 30/08/2013]. Available at: http://www.centronazionalesangue.it/sites/default/files/dd.mm_._12.04.20....
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