Informed Consent Data Collection
Informed Consent Data Collection is a methodological framework within clinical trial data collection that specifically governs the systematic acquisition, documentation, and management of voluntary participant authorizations, distinguishing itself by ensuring ethical compliance, participant understanding of risks and procedures, and regulatory adherence prior to data or biosample acquisition.
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632
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324
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2017–2026
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Informed consent: study of quality of information given to participants in a clinical trial.
Niels Lynöe, Mikael Sandlund, Géraldine Dahlqvist et al. · BMJ · 1991 · 254 citations · Full text
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Inserm
Paris, France
6 h-index
6 publications
399 citations

Karolinska Institutet
Stockholm, Sweden
4 h-index
5 publications
171 citations
Sorbonne Paris Cité
Paris, France
4 h-index
4 publications
294 citations
National Institutes of Health Clinical Center
Bethesda, United States
4 h-index
4 publications
274 citations
Duke University
Durham, United States
4 h-index
8 publications
586 citations
University of Pennsylvania
Philadelphia, United States
4 h-index
7 publications
429 citations
Hôtel-Dieu de Paris
Paris, France
4 h-index
12 publications
882 citations

University of Leicester
Leicester, United Kingdom
4 h-index
34 publications
875 citations
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5 publications · 181 citations
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6 publications · 281 citations
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4 publications · 294 citations
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4 publications · 215 citations
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