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Therapeutic innovation in the European Union: analysis of the drugs approved by the EMEA between 1995 and 2003

Since January 1995, all European Union applications for marketing approval for medicinal products derived from biotechnology and other drugs considered potentially innovative follow the EMEA centralized procedure. In order to assess the overall degree of therapeutic innovation of these drugs, we con...

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Détails bibliographiques
Auteurs principaux: Motola, Domenico, De Ponti, Fabrizio, Rossi, Pasqualino, Martini, Nello, Montanaro, Nicola
Format: Artigo
Langue:Inglês
Publié: Blackwell Science Inc 2005
Sujets:
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC1884813/
https://ncbi.nlm.nih.gov/pubmed/15801943
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1365-2125.2004.02320.x
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