Literature DB >> 32342737

Electronic Informed Consent in Mobile Applications Research.

John T Wilbanks1.   

Abstract

The article covers electronic informed consent (eIC) from different dimensions so that practitioners might understand the history, regulation, and current status of eIC. It covers the transition of informed consent to electronic screens and the implications of that transition in terms of design, costs, and data analysis. The article explores the limits of regulation mandating eIC for mobile application research, and addresses some of the broader social context around eIC.

Mesh:

Year:  2020        PMID: 32342737     DOI: 10.1177/1073110520917040

Source DB:  PubMed          Journal:  J Law Med Ethics        ISSN: 1073-1105            Impact factor:   1.718


  3 in total

1.  21st Century Cures Act: ethical recommendations for new patient-facing products.

Authors:  Brigitte N Durieux; Matthew DeCamp; Charlotta Lindvall
Journal:  J Am Med Inform Assoc       Date:  2022-09-12       Impact factor: 7.942

2.  Written informed consent to virtual e-consent in clinical research: Changing necessity during COVID times.

Authors:  Apoorva Mathur
Journal:  Indian J Pharmacol       Date:  2021 May-Jun       Impact factor: 1.200

3.  Digital phenotyping and sensitive health data: Implications for data governance.

Authors:  Ignacio Perez-Pozuelo; Dimitris Spathis; Jordan Gifford-Moore; Jessica Morley; Josh Cowls
Journal:  J Am Med Inform Assoc       Date:  2021-08-13       Impact factor: 4.497

  3 in total

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