Informed Consent Monitoring

Informed Consent Monitoring is a methodological framework within trial monitoring that systematically verifies the authenticity, comprehension, and voluntariness of participants' consent in clinical or research trials to ensure ethical and regulatory compliance.

30

Publications

876

Citations

144

Authors

96

Institutions

Publications per year

2017–2026

5

Authors

144

  1. JS
    Jeremy Sugarman

    Johns Hopkins University, United States

    3 publications · 178 citations

    3

    h-index

  2. PW
    Philip W. Lavori

    Stanford University, United States

    2 publications · 157 citations

    2

    h-index

  3. SS
    Stan Shapiro

    McGill University, Canada

    2 publications · 68 citations

    2

    h-index

  4. CW
    Charles Weijer

    Western University, Canada

    2 publications · 68 citations

    2

    h-index

  5. JV
    James V. Lavery

    University of Toronto, Canada

    1 publications · 21 citations

    1

    h-index

1–5 of 144

Venues

  1. PubMed

    Repository · 2 publications · 93 citations

    2

    h-index

  2. Clinical Trials

    2 publications · 157 citations

    2

    h-index

  3. BMJ

    2 publications · 64 citations

    2

    h-index

  4. IRB Ethics and Human Research

    2 publications · 32 citations

    2

    h-index

  5. Indian Journal of Medical Ethics

    1 publications · 15 citations

    1

    h-index

1–5