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Journal of Medical Internet Research
|
August 5, 2020
Landscape of Participant-Centric Initiatives for Medical Research in the United States, the United Kingdom, and Japan: Scoping Review
Nao Hamakawa, Rumiko Nakano, Atsushi Kogetsu, et al.
BMJ (Clinical Research Ed.)
|
February 7, 2014
A dynamic model of patient consent to sharing of medical record data
William G Dixon, Karen Spencer, Hawys Williams, et al.
Journal of Law and the Biosciences
|
July 7, 2022
Biomodifying the 'natural': from Adaptive Regulation to Adaptive Societal Governance
Miranda Mourby, Jessica Bell, Michael Morrison, et al.
JMIR Medical Informatics
|
January 15, 2015
Dynamic consent: a possible solution to improve patient confidence and trust in how electronic patient records are used in medical research
Hawys Williams, Karen Spencer, Caroline Sanders, et al.
Digital Health
|
June 27, 2018
Making the most of the waiting room: Electronic patient engagement, a mixed methods study
Victoria Coathup, Teresa Finlay, Harriet Ja Teare, et al.
BMC Medical Ethics
|
October 14, 2016
Personalized assent for pediatric biobanks
Noor A A Giesbertz, Karen Melham, Jane Kaye, et al.
BMC Pregnancy and Childbirth
|
September 25, 2016
eRegistries: governance for electronic maternal and child health registries
Sonja L Myhre, Jane Kaye, Lee A Bygrave, et al.
Plos Genetics
|
October 3, 2009
Public access to genome-wide data: five views on balancing research with privacy and protection
, George Church, Catherine Heeney, et al.
BMC Medical Ethics
|
August 25, 2016
Using digital technologies to engage with medical research: views of myotonic dystrophy patients in Japan
Victoria Coathup, Harriet J A Teare, Jusaku Minari, et al.
Journal of Law and Medicine
|
January 8, 2021
Don Chalmers: His Contributions to Legal Research and Education, Health Law, and Research Ethics, Locally and Globally
Dianne Nicol, Yann Joly, Jane Kaye, et al.
Page
of 10
Search research articles
Search
Showing results (41-50 of 99) with videos related to
Sort By:
Page
of 10
Journal of Medical Internet Research
|
August 5, 2020
Landscape of Participant-Centric Initiatives for Medical Research in the United States, the United Kingdom, and Japan: Scoping Review
Nao Hamakawa, Rumiko Nakano, Atsushi Kogetsu, et al.
BMJ (Clinical Research Ed.)
|
February 7, 2014
A dynamic model of patient consent to sharing of medical record data
William G Dixon, Karen Spencer, Hawys Williams, et al.
Journal of Law and the Biosciences
|
July 7, 2022
Biomodifying the 'natural': from Adaptive Regulation to Adaptive Societal Governance
Miranda Mourby, Jessica Bell, Michael Morrison, et al.
JMIR Medical Informatics
|
January 15, 2015
Dynamic consent: a possible solution to improve patient confidence and trust in how electronic patient records are used in medical research
Hawys Williams, Karen Spencer, Caroline Sanders, et al.
Digital Health
|
June 27, 2018
Making the most of the waiting room: Electronic patient engagement, a mixed methods study
Victoria Coathup, Teresa Finlay, Harriet Ja Teare, et al.
BMC Medical Ethics
|
October 14, 2016
Personalized assent for pediatric biobanks
Noor A A Giesbertz, Karen Melham, Jane Kaye, et al.
BMC Pregnancy and Childbirth
|
September 25, 2016
eRegistries: governance for electronic maternal and child health registries
Sonja L Myhre, Jane Kaye, Lee A Bygrave, et al.
Plos Genetics
|
October 3, 2009
Public access to genome-wide data: five views on balancing research with privacy and protection
, George Church, Catherine Heeney, et al.
BMC Medical Ethics
|
August 25, 2016
Using digital technologies to engage with medical research: views of myotonic dystrophy patients in Japan
Victoria Coathup, Harriet J A Teare, Jusaku Minari, et al.
Journal of Law and Medicine
|
January 8, 2021
Don Chalmers: His Contributions to Legal Research and Education, Health Law, and Research Ethics, Locally and Globally
Dianne Nicol, Yann Joly, Jane Kaye, et al.
Page
of 10