Views of clinical trial participants on the readability and their understanding of informed consent documents

R Sommers, C Van Staden, F Steffens - AJOB Empirical Bioethics, 2017 - Taylor & Francis
Background: One of the ethical imperatives for a valid consent process in clinical medication
trials is that the process be guided by and recorded in an informed consent document (ICD) …
被引用次数：11 相关文章

Views of clinical trial participants on the readability and their understanding of informed consent documents

R Somers, C Van Staden… - AJOB empirical …, 2017 - pubmed.ncbi.nlm.nih.gov
Background One of the ethical imperatives for a valid consent process in clinical medication
trials is that the process be guided by and recorded in an informed consent document (ICD) …

Views of clinical trial participants on the readability and their understanding of informed consent documents.

R Somers, C Van Staden, F Steffens - AJOB Empirical Bioethics, 2017 - europepmc.org
Background One of the ethical imperatives for a valid consent process in clinical medication
trials is that the process be guided by and recorded in an informed consent document (ICD) …
[PDF] researchgate.net

[PDF][PDF] Views of clinical trial participants on the readability and their understanding of informed consent documents

R Somers, C Van Staden, F Steffens - 2017 - researchgate.net
Background: One of the ethical imperatives for a valid consent process in clinical medication
trials is that the process be guided by and recorded in an informed consent document (ICD) …

Views of clinical trial participants on the readability and their understanding of informed consent documents

R Sommers, C Van Staden, F Steffens - Ajob Empirical Bioethics, 2017 - philpapers.org
Background: One of the ethical imperatives for a valid consent process in clinical medication
trials is that the process be guided by and recorded in an informed consent document (ICD) …