Four reasons why too many informed consents to clinical research are invalid: a critical analysis of current practices

OBJECTIVE: Informed consent (IC) is a central ethical and legal requirement for clinical research that aims to protect the autonomy of participants. To enable an autonomous decision and valid consent, adequate understanding must be ensured. However, a considerable proportion of participants do not u...

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Detalles Bibliográficos
Autores principales: Wisgalla, Anne, Hasford, Joerg
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2022
Materias:
Ethics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8900041/
https://www.ncbi.nlm.nih.gov/pubmed/35246415
http://dx.doi.org/10.1136/bmjopen-2021-050543

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8900041/
https://www.ncbi.nlm.nih.gov/pubmed/35246415
http://dx.doi.org/10.1136/bmjopen-2021-050543

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