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The Journal of Pediatrics
|
August 17, 2002
The ethics of paying for children's participation in research
David Wendler, Jonathan E Rackoff, Ezekiel J Emanuel, et al.
JAMA
|
August 18, 2005
Quantifying the federal minimal risk standard: implications for pediatric research without a prospect of direct benefit
David Wendler, Leah Belsky, Kimberly M Thompson, et al.
JAMA
|
January 30, 2004
How do institutional review boards apply the federal risk and benefit standards for pediatric research?
Seema Shah, Amy Whittle, Benjamin Wilfond, et al.
Archives of Internal Medicine
|
April 28, 2010
Is emergency research without initial consent justified?: the consent substitute model
Emily A Largent, David Wendler, Ezekiel Emanuel, et al.
British Journal of Clinical Pharmacology
|
April 19, 2017
Public preferences on written informed consent for low-risk pragmatic clinical trials in Spain
Rafael Dal-Ré, Antonio J Carcas, Xavier Carné, et al.
AIDS (London, England)
|
November 16, 2010
Empirical evaluation of the need for 'on-going consent' in clinical research
William Smith, Christine Grady, Benjamin Krohmal, et al.
BMC Medical Research Methodology
|
September 20, 2017
Patients' beliefs regarding informed consent for low-risk pragmatic trials
Rafael Dal-Ré, Antonio J Carcas, Xavier Carné, et al.
Pediatrics
|
June 3, 2004
Institutional review board practices regarding assent in pediatric research
Amy Whittle, Seema Shah, Benjamin Wilfond, et al.
The American Journal of Bioethics : AJOB
|
June 30, 2017
A Proposed Process for Reliably Updating the Common Rule
Benjamin E Berkman, David Wendler, Haley K Sullivan, et al.
AJOB Empirical Bioethics
|
March 23, 2016
Adolescent Research Participants' Descriptions of Medical Research
Christine Grady, Isabella Nogues, Lori Wiener, et al.
Page
of 22
Search research articles
Search
Showing results (151-160 of 214) with videos related to
Sort By:
Page
of 22
The Journal of Pediatrics
|
August 17, 2002
The ethics of paying for children's participation in research
David Wendler, Jonathan E Rackoff, Ezekiel J Emanuel, et al.
JAMA
|
August 18, 2005
Quantifying the federal minimal risk standard: implications for pediatric research without a prospect of direct benefit
David Wendler, Leah Belsky, Kimberly M Thompson, et al.
JAMA
|
January 30, 2004
How do institutional review boards apply the federal risk and benefit standards for pediatric research?
Seema Shah, Amy Whittle, Benjamin Wilfond, et al.
Archives of Internal Medicine
|
April 28, 2010
Is emergency research without initial consent justified?: the consent substitute model
Emily A Largent, David Wendler, Ezekiel Emanuel, et al.
British Journal of Clinical Pharmacology
|
April 19, 2017
Public preferences on written informed consent for low-risk pragmatic clinical trials in Spain
Rafael Dal-Ré, Antonio J Carcas, Xavier Carné, et al.
AIDS (London, England)
|
November 16, 2010
Empirical evaluation of the need for 'on-going consent' in clinical research
William Smith, Christine Grady, Benjamin Krohmal, et al.
BMC Medical Research Methodology
|
September 20, 2017
Patients' beliefs regarding informed consent for low-risk pragmatic trials
Rafael Dal-Ré, Antonio J Carcas, Xavier Carné, et al.
Pediatrics
|
June 3, 2004
Institutional review board practices regarding assent in pediatric research
Amy Whittle, Seema Shah, Benjamin Wilfond, et al.
The American Journal of Bioethics : AJOB
|
June 30, 2017
A Proposed Process for Reliably Updating the Common Rule
Benjamin E Berkman, David Wendler, Haley K Sullivan, et al.
AJOB Empirical Bioethics
|
March 23, 2016
Adolescent Research Participants' Descriptions of Medical Research
Christine Grady, Isabella Nogues, Lori Wiener, et al.
Page
of 22