2022
Regulating Posttrial Access to In-Dwelling Class III Neural Devices
Wright M, Fins J. Regulating Posttrial Access to In-Dwelling Class III Neural Devices. 2022, 256-267. DOI: 10.1017/9781108975452.020.Peer-Reviewed Original ResearchMedical device regulationRegulatory lawsDevice regulationCambridge CorePosttrial accessMedical devicesRegulatory concernsOpen AccessPatient privacyRegulationPublic healthMedical providersLawInnovative productsEUBookConcernsControversiesPrivacyPolicymakersAccessUSStakeholdersCambridgeMultidisciplinary evaluation
2016
The Effects of Closed-Loop Medical Devices on the Autonomy and Accountability of Persons and Systems
Kellmeyer P, Cochrane T, Müller O, Mitchell C, Ball T, Fins J, Biller-Andorno N. The Effects of Closed-Loop Medical Devices on the Autonomy and Accountability of Persons and Systems. Cambridge Quarterly Of Healthcare Ethics 2016, 25: 623-633. PMID: 27634714, DOI: 10.1017/s0963180116000359.Peer-Reviewed Original ResearchConceptsClosed-loop medical devicesRepresentatives of patient advocacy groupsMedical lawLegal accountabilityLegal frameworkDecisionmaking capacityRestoring communication abilitiesPersonal autonomyMedical ethicsPatient autonomyMedical devicesAdvocacy groupsAutonomyMedical neuroscienceTask ForceAccountsPatient advocacy groupsPersonsLawConsentComputer scienceRefusalDecisionmakingEthicsAgencies