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
12
The need for transparency of clinical evidence for medical devices in Europe
Alan G. Fraser, Eric G. Butchart, Piotr Szymański et al. · The Lancet · 2018 · 101 citations · Full text
Law, Health Law, Health Policy +14
1–5 of 12
41
1
h-index
1
h-index
1
h-index
1
h-index
1
h-index
1–5 of 41
29
Politecnico di Milano
Milan, Italy
1 h-index
1 publications
101 citations
Albert Einstein College of Medicine
Bronx, United States
1 h-index
2 publications
34 citations
Telefonica Research and Development
Madrid, Spain
1 h-index
1 publications
18 citations
Harry Perkins Institute of Medical Research
Nedlands, Australia
1 h-index
1 publications
24 citations

Macquarie University
Sydney, Australia
1 h-index
5 publications
120 citations

Chapel Allerton Hospital
Leeds, United Kingdom
1 h-index
3 publications
96 citations
Memorial University of Newfoundland
St. John's, Canada
1 h-index
1 publications
47 citations
Australian Institute of Health and Welfare
Canberra, Australia
1 h-index
2 publications
48 citations
1–8 of 29
2 publications · 119 citations
2
h-index
1 publications · 32 citations
1
h-index
IJO · 1 publications · 32 citations
1
h-index
1 publications · 17 citations
1
h-index
1 publications · 85 citations
1
h-index
1–5