The regulation of cognitive enhancement devices : extending the medical model

This article presents a model for regulating cognitive enhancement devices (CEDs). Recently, it has become very easy for individuals to purchase devices which directly modulate brain function. For example, transcranial direct current stimulators are increasingly being produced and marketed online as...

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Détails bibliographiques
Auteurs principaux: Maslen, H, Douglas, T, Cohen Kadosh, R, Levy, N, Savulescu, J
Format: Journal article
Langue:English
Publié: Oxford University Press 2014
Sujets:
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author Maslen, H
Douglas, T
Cohen Kadosh, R
Levy, N
Savulescu, J
author_facet Maslen, H
Douglas, T
Cohen Kadosh, R
Levy, N
Savulescu, J
author_sort Maslen, H
collection OXFORD
description This article presents a model for regulating cognitive enhancement devices (CEDs). Recently, it has become very easy for individuals to purchase devices which directly modulate brain function. For example, transcranial direct current stimulators are increasingly being produced and marketed online as devices for cognitive enhancement. Despite posing risks in a similar way to medical devices, devices that do not make any therapeutic claims do not have to meet anything more than basic product safety standards. We present the case for extending existing medical device legislation to cover CEDs. Medical devices and CEDs operate by the same or similar mechanisms and pose the same or similar risks. This fact coupled with the arbitrariness of the line between treatment and enhancement count in favour of regulating these devices in the same way. In arguing for this regulatory model, the paper highlights potential challenges to its implementation, and suggests solutions.
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spelling oxford-uuid:6c191dc3-3c76-41fa-b13c-e34e02cdfb1f2022-03-26T19:08:41ZThe regulation of cognitive enhancement devices : extending the medical modelJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:6c191dc3-3c76-41fa-b13c-e34e02cdfb1fEthics (Moral philosophy)Ethics of the biosciencesPhilosophyPractical ethicsEnglishOxford University Research Archive - ValetOxford University Press2014Maslen, HDouglas, TCohen Kadosh, RLevy, NSavulescu, JThis article presents a model for regulating cognitive enhancement devices (CEDs). Recently, it has become very easy for individuals to purchase devices which directly modulate brain function. For example, transcranial direct current stimulators are increasingly being produced and marketed online as devices for cognitive enhancement. Despite posing risks in a similar way to medical devices, devices that do not make any therapeutic claims do not have to meet anything more than basic product safety standards. We present the case for extending existing medical device legislation to cover CEDs. Medical devices and CEDs operate by the same or similar mechanisms and pose the same or similar risks. This fact coupled with the arbitrariness of the line between treatment and enhancement count in favour of regulating these devices in the same way. In arguing for this regulatory model, the paper highlights potential challenges to its implementation, and suggests solutions.
spellingShingle Ethics (Moral philosophy)
Ethics of the biosciences
Philosophy
Practical ethics
Maslen, H
Douglas, T
Cohen Kadosh, R
Levy, N
Savulescu, J
The regulation of cognitive enhancement devices : extending the medical model
title The regulation of cognitive enhancement devices : extending the medical model
title_full The regulation of cognitive enhancement devices : extending the medical model
title_fullStr The regulation of cognitive enhancement devices : extending the medical model
title_full_unstemmed The regulation of cognitive enhancement devices : extending the medical model
title_short The regulation of cognitive enhancement devices : extending the medical model
title_sort regulation of cognitive enhancement devices extending the medical model
topic Ethics (Moral philosophy)
Ethics of the biosciences
Philosophy
Practical ethics
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