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.
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Publications
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Authors
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Institutions
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2017–2026
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Animal Testing AlternativesBiocompatible Material SelectionBiological Evaluation PlanningBiological Evaluation ReportBiological Safety EndpointsClinical Biocompatibility AssessmentCorrosion Biological EffectsDevice-patient Interaction AssessmentIntracutaneous ReactivityMaterial-mediated Toxicity
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Implantable Devices: Issues and Challenges
Kateryna Bazaka, Mohan V. Jacob · Electronics · 2012 · 350 citations · Full text
Sarah Gruber, Angela Nickel · Frontiers in Medical Technology · 2023 · 144 citations · Full text
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Forest Institute
Springfield, United States
3 h-index
3 publications
100 citations

University of Alberta
Edmonton, Canada
2 h-index
3 publications
169 citations
Inserm
Paris, France
2 h-index
7 publications
233 citations
Northwestern University
Evanston, United States
1 h-index
1 publications
12 citations
Freie Universität Berlin
Berlin, Germany
1 h-index
1 publications
15 citations
The Hunterian
Glasgow, United Kingdom
1 h-index
2 publications
88 citations
Queen's Medical Centre
Nottingham, United Kingdom
1 h-index
3 publications
1.1K citations
Sungkyunkwan University
Seoul, South Korea
1 h-index
1 publications
115 citations
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Repository · 5 publications · 108 citations
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2 publications · 52 citations
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2 publications · 145 citations
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2 publications · 33 citations
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