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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...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BMJ Publishing Group
2022
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| 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 |