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Pharmaceutical Statistics
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July 12, 2022
Informed decision-making: Statistical methodology for surrogacy evaluation and its role in licensing and reimbursement assessments
Christopher J Weir, Rod S Taylor
Pharmaceutical Statistics
|
October 7, 2010
Optimal caliper widths for propensity-score matching when estimating differences in means and differences in proportions in observational studies
Peter C Austin
Pharmaceutical Statistics
|
October 23, 2010
Review of the statistical analysis of the dog telemetry study
Mike Aylott, Simon Bate, Susie Collins, et al.
Pharmaceutical Statistics
|
August 26, 2010
Practical issues and lessons learned from multi-regional clinical trials via case examples: a Japanese perspective
Yuki Ando, Toshimitsu Hamasaki
Pharmaceutical Statistics
|
February 11, 2011
Additional results for 'Sequential design approaches for bioequivalence studies with crossover designs'
Timothy H Montague, Diane Potvin, Charles E Diliberti, et al.
Pharmaceutical Statistics
|
January 27, 2011
A new mathematical approach for the estimation of the AUC and its variability under different experimental designs in preclinical studies
Carmen Navarro-Fontestad, Isabel González-Álvarez, Carlos Fernández-Teruel, et al.
Pharmaceutical Statistics
|
June 23, 2010
Proposals of statistical consideration to evaluation of results for a specific region in multi-regional trials--Asian perspective
Hsiao-Hui Tsou, Shein-Chung Chow, K K Gordon Lan, et al.
Pharmaceutical Statistics
|
January 29, 2011
Making available information from studies sponsored by the pharmaceutical industry: some current practices
Michael O'Kelly, Steven A Julious, Stephen Pyke, et al.
Pharmaceutical Statistics
|
January 29, 2011
Commentary
Steven Snapinn
Pharmaceutical Statistics
|
March 24, 2021
A simulation-free group sequential design with max-combo tests in the presence of non-proportional hazards
Lili Wang, Xiaodong Luo, Cheng Zheng
Page
of 124
Search research articles
Search
Showing results (11-20 of 1,234) with videos related to
Sort By:
Page
of 124
Pharmaceutical Statistics
|
July 12, 2022
Informed decision-making: Statistical methodology for surrogacy evaluation and its role in licensing and reimbursement assessments
Christopher J Weir, Rod S Taylor
Pharmaceutical Statistics
|
October 7, 2010
Optimal caliper widths for propensity-score matching when estimating differences in means and differences in proportions in observational studies
Peter C Austin
Pharmaceutical Statistics
|
October 23, 2010
Review of the statistical analysis of the dog telemetry study
Mike Aylott, Simon Bate, Susie Collins, et al.
Pharmaceutical Statistics
|
August 26, 2010
Practical issues and lessons learned from multi-regional clinical trials via case examples: a Japanese perspective
Yuki Ando, Toshimitsu Hamasaki
Pharmaceutical Statistics
|
February 11, 2011
Additional results for 'Sequential design approaches for bioequivalence studies with crossover designs'
Timothy H Montague, Diane Potvin, Charles E Diliberti, et al.
Pharmaceutical Statistics
|
January 27, 2011
A new mathematical approach for the estimation of the AUC and its variability under different experimental designs in preclinical studies
Carmen Navarro-Fontestad, Isabel González-Álvarez, Carlos Fernández-Teruel, et al.
Pharmaceutical Statistics
|
June 23, 2010
Proposals of statistical consideration to evaluation of results for a specific region in multi-regional trials--Asian perspective
Hsiao-Hui Tsou, Shein-Chung Chow, K K Gordon Lan, et al.
Pharmaceutical Statistics
|
January 29, 2011
Making available information from studies sponsored by the pharmaceutical industry: some current practices
Michael O'Kelly, Steven A Julious, Stephen Pyke, et al.
Pharmaceutical Statistics
|
January 29, 2011
Commentary
Steven Snapinn
Pharmaceutical Statistics
|
March 24, 2021
A simulation-free group sequential design with max-combo tests in the presence of non-proportional hazards
Lili Wang, Xiaodong Luo, Cheng Zheng
Page
of 124