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Monitoring product safety in the postmarketing environment
The safety profile of a medicinal product may change in the postmarketing environment. Safety issues not identified in clinical development may be seen and need to be evaluated. Methods of evaluating spontaneous adverse experience reports and identifying new safety risks include a review of individu...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
SAGE Publications
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4125313/ https://ncbi.nlm.nih.gov/pubmed/25114782 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/2042098613490780 |
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