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Access to regulatory data from the European Medicines Agency: the times they are a-changing
Systematic reviewers are increasingly trying to obtain regulatory clinical study reports (CSRs) to correct for publication bias. For instance, our organization, the Institute for Quality and Efficiency in Health Care, routinely asks drug manufacturers to provide full CSRs of studies considered in he...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3495027/ https://ncbi.nlm.nih.gov/pubmed/23110993 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/2046-4053-1-50 |
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