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    Ethical and legal implications for technological devices in clinical research in Europe: Flowchart design for ethical and legal decisions in clinical research

    Identifiers
    URI: http://hdl.handle.net/11556/1184
    ISBN: 978-145037597-9
    DOI: 10.1145/3471391.3471403
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    Author/s
    Garzo, Ainara; Garay-Vitoria, Nestor
    Date
    2021-09
    Keywords
    Competent authority
    Ethical committee
    Informed consent
    Privacy
    User studies
    Abstract
    In recent years engineers developing new technologies with assistive or medical purposes have become aware that to create acceptable and usable solutions they need to involve final users, patients and stakeholders in the design, development and evaluation of systems as well as in the device certification processes. Involving stakeholders in such processes has several ethical and legal implications. It has become evident that it is still difficult for engineers in Europe to know which ethical and legal processes should be carried out as they have not been previously trained in these issues during their studies. This article is a review of the laws, standards and recommendations applicable in Europe concerning human involvement in new technologies research, with the aim of helping researchers in the region in question to identify the ethical and legal issues that could arise during those tasks. This review has been carried out in response to the identified need on the part of technological ...
    Type
    conferenceObject

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