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Aspects of vulnerable patients and informed consent in clinical trials
Scope: To discuss the rationale behind informed consent in clinical trials focusing on vulnerable patients from a European and German viewpoint. Methods: Scientific literature search via PubMed, Medline, Google. Results: Voluntary informed consent is the cornerstone of policies regulating clinical t...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
German Medical Science GMS Publishing House
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3551442/ https://ncbi.nlm.nih.gov/pubmed/23346043 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3205/000171 |
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