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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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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Dove Medical Press
2009
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3108683/ https://ncbi.nlm.nih.gov/pubmed/21701609 |
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