European legislation impedes critical care research and fails to protect patients' rights

The European Clinical Trials Directive requires an informed consent from the patient or a proxy in drug trials. Although informed consent is a valuable tool to protect patients' rights in clinical trials, this requirement largely impedes research in critical care settings, and if pursued in thi...

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Detalles Bibliográficos
Autores principales: Berg, Ronan MG, Møller, Kirsten, Rossel, Peter J Hancke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Commentary
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3219370/
https://www.ncbi.nlm.nih.gov/pubmed/21542880
http://dx.doi.org/10.1186/cc10113

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3219370/
https://www.ncbi.nlm.nih.gov/pubmed/21542880
http://dx.doi.org/10.1186/cc10113

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