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Journal of Clinical Epidemiology
|
July 14, 2020
Achieving effective informed oversight by DMCs in COVID clinical trials
David L DeMets, Thomas R Fleming
Clinical Trials (London, England)
|
June 16, 2006
An Institutional Review Board dilemma: responsible for safety monitoring but not in control
David L DeMets, Norman Fost, Madison Powers
Biometrics
|
March 23, 2004
Design and analysis of group sequential clinical trials with multiple primary endpoints
Michael R Kosorok, Shi Yuanjun, David L DeMets
Statistics in Medicine
|
September 27, 2002
Monitoring clinical trials: issues and controversies regarding confidentiality
Thomas R Fleming, Susan Ellenberg, David L DeMets
Biostatistics (Oxford, England)
|
June 22, 2017
Discussion: The role, position, and function of the FDA-The past, present, and future
Thomas R Fleming, David L Demets, Lisa M McShane
Journal of Allergy and Infectious Diseases
|
January 10, 2022
Monitoring clinical trials in infectious diseases
David L DeMets, Thomas R Fleming, Susan S Ellenberg
JAMA
|
July 15, 2010
Bias and trials stopped early for benefit
Susan S Ellenberg, David L DeMets, Thomas R Fleming
Clinical Trials (London, England)
|
April 10, 2018
Data Monitoring Committees: Current issues
Thomas R Fleming, Susan S Ellenberg, David L DeMets
JAMA
|
February 28, 2020
When Can Intermediate Outcomes Be Used as Surrogate Outcomes?
David L DeMets, Bruce M Psaty, Thomas R Fleming
Clinical Trials (London, England)
|
March 30, 2024
Society for Clinical Trials Data Monitoring Committee initiative website: Closing the gap
David L DeMets, Susan Halabi, Lehana Thabane, et al.
Page
of 10
Search research articles
Search
Showing results (21-30 of 98) with videos related to
Sort By:
Page
of 10
Journal of Clinical Epidemiology
|
July 14, 2020
Achieving effective informed oversight by DMCs in COVID clinical trials
David L DeMets, Thomas R Fleming
Clinical Trials (London, England)
|
June 16, 2006
An Institutional Review Board dilemma: responsible for safety monitoring but not in control
David L DeMets, Norman Fost, Madison Powers
Biometrics
|
March 23, 2004
Design and analysis of group sequential clinical trials with multiple primary endpoints
Michael R Kosorok, Shi Yuanjun, David L DeMets
Statistics in Medicine
|
September 27, 2002
Monitoring clinical trials: issues and controversies regarding confidentiality
Thomas R Fleming, Susan Ellenberg, David L DeMets
Biostatistics (Oxford, England)
|
June 22, 2017
Discussion: The role, position, and function of the FDA-The past, present, and future
Thomas R Fleming, David L Demets, Lisa M McShane
Journal of Allergy and Infectious Diseases
|
January 10, 2022
Monitoring clinical trials in infectious diseases
David L DeMets, Thomas R Fleming, Susan S Ellenberg
JAMA
|
July 15, 2010
Bias and trials stopped early for benefit
Susan S Ellenberg, David L DeMets, Thomas R Fleming
Clinical Trials (London, England)
|
April 10, 2018
Data Monitoring Committees: Current issues
Thomas R Fleming, Susan S Ellenberg, David L DeMets
JAMA
|
February 28, 2020
When Can Intermediate Outcomes Be Used as Surrogate Outcomes?
David L DeMets, Bruce M Psaty, Thomas R Fleming
Clinical Trials (London, England)
|
March 30, 2024
Society for Clinical Trials Data Monitoring Committee initiative website: Closing the gap
David L DeMets, Susan Halabi, Lehana Thabane, et al.
Page
of 10