Device Accountability

Device Accountability is a regulatory requirement within investigational device exemptions that mandates the systematic tracking and documentation of an investigational medical device’s disposition, use, and location throughout its lifecycle to ensure compliance with ethical, legal, and scientific standards.

12

Publications

492

Citations

41

Authors

29

Institutions

Publications per year

2017–2026

8

Variants

Investigational Device Accountability

Authors

41

  1. TB
    Tonio Ball

    University of Freiburg, Germany

    1 publications · 85 citations

    1

    h-index

  2. BB
    Brette Blakely

    Macquarie University, Australia

    1 publications · 24 citations

    1

    h-index

  3. SS
    S. S. Dhruva

    University of California, San Francisco, United States

    1 publications · 17 citations

    1

    h-index

  4. SC
    Scott Crosby

    NHS Forth Valley, United Kingdom

    1 publications · 101 citations

    1

    h-index

  5. FV
    Frans Van de Werf

    KU Leuven, Belgium

    1 publications · 101 citations

    1

    h-index

1–5 of 41

Venues

  1. The Lancet

    2 publications · 119 citations

    2

    h-index

  2. Ophthalmology and Therapy

    1 publications · 32 citations

    1

    h-index

  3. Indian Journal of Orthopaedics

    IJO · 1 publications · 32 citations

    1

    h-index

  4. BMJ

    1 publications · 17 citations

    1

    h-index

  5. Cambridge Quarterly of Healthcare Ethics

    1 publications · 85 citations

    1

    h-index

1–5