Device Vigilance

Device Vigilance is a systematic post-market surveillance framework designed to monitor, detect, assess, and report adverse events and safety signals associated with medical devices after their release into the market, distinguishing it from broader regulatory compliance activities by focusing specifically on early identification and mitigation of risks to patient safety.

22

Publications

840

Citations

104

Authors

58

Institutions

Publications per year

2017–2026

4

Authors

104

  1. WH
    William H. Maisel

    Brigham and Women's Hospital, United States

    2 publications · 235 citations

    2

    h-index

  2. JW
    James W. Cox

    University of Maryland, Baltimore, United States

    2 publications · 51 citations

    2

    h-index

  3. JG
    John Gimbel

    University of Alaska Fairbanks, United States

    2 publications · 51 citations

    2

    h-index

  4. EC
    Elizabeth Ching

    Cleveland Clinic, United States

    1 publications · 177 citations

    1

    h-index

  5. ET
    Enno T. van der Velde

    Leiden University Medical Center, Netherlands

    1 publications · 16 citations

    1

    h-index

1–5 of 104

Venues

  1. Mayo Clinic Proceedings

    2 publications · 51 citations

    2

    h-index

  2. PubMed

    Repository · 2 publications · 74 citations

    2

    h-index

  3. 1

    h-index

  4. British Journal of Ophthalmology

    BJO · 1 publications · 14 citations

    1

    h-index

  5. Smart Health

    1 publications · 26 citations

    1

    h-index

1–5