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.

114

Publications

5.7K

Citations

632

Authors

324

Institutions

Publications per year

2017–2026

38

Authors

632

  1. PR
    Philippe Ravaud

    Université Paris Cité, France

    5 publications · 349 citations

    5

    h-index

  2. MB
    Mehdi Benchoufi

    Inserm, France

    5 publications · 349 citations

    5

    h-index

  3. SY
    Scott Y. H. Kim

    University of Michigan, United States

    3 publications · 100 citations

    3

    h-index

  4. CW
    Charles Weijer

    Western University, Canada

    3 publications · 96 citations

    3

    h-index

  5. RP
    Raphaël Porcher

    Université Paris Cité, France

    3 publications · 243 citations

    3

    h-index

1–5 of 632

Venues

  1. Clinical Trials

    5 publications · 181 citations

    5

    h-index

  2. PLoS ONE

    6 publications · 281 citations

    5

    h-index

  3. BMJ

    4 publications · 327 citations

    4

    h-index

  4. F1000Research

    4 publications · 294 citations

    4

    h-index

  5. Journal of Medical Ethics

    4 publications · 215 citations

    4

    h-index

1–5