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Information technology in pharmacovigilance: Benefits, challenges, and future directions from industry perspectives

Risk assessment during clinical product development needs to be conducted in a thorough and rigorous manner. However, it is impossible to identify all safety concerns during controlled clinical trials. Once a product is marketed, there is generally a large increase in the number of patients exposed,...

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Dettagli Bibliografici
Autore principale: Lu, Zhengwu
Natura: Artigo
Lingua:Inglês
Pubblicazione: Dove Medical Press 2009
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC3108683/
https://ncbi.nlm.nih.gov/pubmed/21701609
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