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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Detalles Bibliográficos
Autores principales: Kuthning, Maria, Hundt, Ferdinand
Formato: Online Artículo Texto
Lenguaje:English
Publicado: German Medical Science GMS Publishing House 2013
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3551442/
https://www.ncbi.nlm.nih.gov/pubmed/23346043
http://dx.doi.org/10.3205/000171

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3551442/
https://www.ncbi.nlm.nih.gov/pubmed/23346043
http://dx.doi.org/10.3205/000171

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