Evaluations of medical device usability during clinical investigations: a scoping review of clinical study protocols

Author:

Douze Laura12ORCID,Schiro Jessica12,Heyndels Louise2,Pazart Lionel3,Pelayo Sylvia12

Affiliation:

1. Évaluation des technologies de santé et des pratiques médicales, University Lille, CHU Lille, ULR 2694 - METRICS, Lille, France

2. Inserm, CIC-IT 1403, Lille, France

3. INSERM CIC 1431, Centre d’Investigation Clinique, Centre Hospitalier Universitaire de Besançon, Besancon, France

Publisher

Informa UK Limited

Reference25 articles.

1. Regulation (EU) 2017/745 of the European parliament and of the council of 5 April 2017 on medical devices. 2017 [cited 2024 Jan 15]. Available from: https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=CELEX:32017R0745

2. Impact of Design on Medical Device Safety

3. The effect of design on the usability and real world effectiveness of medical devices: A case study with adolescent users

4. Handbook of Human Factors in Medical Device Design

5. Thimbleby H. Improving safety in medical devices and systems. In: 2013 IEEE International Conference on Healthcare Informatics; Philadelphia, PA (USA). IEEE. p. 1–13.

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