Biocompatibility Requirements

Biocompatibility Requirements is the subset of medical device regulatory requirements that prescribes the legal and technical criteria for assessing and demonstrating that a device’s materials and design do not elicit unacceptable local or systemic biological responses in humans under its intended conditions of use.

54

Publications

3.1K

Citations

220

Authors

97

Institutions

Publications per year

2017–2026

14

Authors

220

  1. DF
    David F. Williams

    Forest Institute, United States

    4 publications · 219 citations

    4

    h-index

  2. CB
    C. Baquey

    Inserm, France

    2 publications · 68 citations

    2

    h-index

  3. MT
    Martti Talja

    Päijät-Hämeen Keskussairaala, Finland

    2 publications · 45 citations

    2

    h-index

  4. RK
    Raju Kammula

    1 publications · 15 citations

    1

    h-index

  5. MV
    Maria Vlad

    Grigore T. Popa University of Medicine and Pharmacy, Romania

    1 publications · 41 citations

    1

    h-index

1–5 of 220

Venues

  1. PubMed

    Repository · 5 publications · 108 citations

    5

    h-index

  2. Biomaterials

    2 publications · 52 citations

    2

    h-index

  3. 2

    h-index

  4. Journal of Biomedical Engineering

    2 publications · 145 citations

    2

    h-index

  5. Journal of Artificial Organs

    2 publications · 33 citations

    2

    h-index

1–5