scholarly journals On the Possibility of Reducing the Sample Size for Microbiological Examination of Some Pharmaceutical Substances

Author(s):  
M. V. Roshchina ◽  
O. V. Gunar ◽  
I. A. Builova
2005 ◽  
Vol 112 (1) ◽  
pp. 268-279 ◽  
Author(s):  
Richard B. Anderson ◽  
Michael E. Doherty ◽  
Neil D. Berg ◽  
Jeff C. Friedrich
Keyword(s):  

2011 ◽  
Author(s):  
M. Lopez-Ramon ◽  
C. Castro ◽  
J. Roca ◽  
J. Lupianez

2009 ◽  
Author(s):  
Dennis L. Jackson ◽  
Marc Frey ◽  
Jennifer Voth
Keyword(s):  

2007 ◽  
Author(s):  
Natalie A. Obrecht ◽  
Gretchen B. Chapman ◽  
Rochel Gelman

1990 ◽  
Vol 29 (03) ◽  
pp. 243-246 ◽  
Author(s):  
M. A. A. Moussa

AbstractVarious approaches are considered for adjustment of clinical trial size for patient noncompliance. Such approaches either model the effect of noncompliance through comparison of two survival distributions or two simple proportions. Models that allow for variation of noncompliance and event rates between time intervals are also considered. The approach that models the noncompliance adjustment on the basis of survival functions is conservative and hence requires larger sample size. The model to be selected for noncompliance adjustment depends upon available estimates of noncompliance and event rate patterns.


Sign in / Sign up

Export Citation Format

Share Document