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A New Look at Informed Consent for Cancer Clinical Trials
Informed consent is fundamental to the conduct of clinical trials. Prospective participants need to be adequately informed and given the opportunity to ask questions and consult with relatives or friends without feeling pressured or rushed.
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| Hoofdauteurs: | , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
American Society of Clinical Oncology
2011
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3140452/ https://ncbi.nlm.nih.gov/pubmed/22043194 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1200/JOP.2011.000347 |
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