
Design and Analysis of Bioavailability and Bioequivalence Studies
679,-

Methodologies in Biosimilar Product Development
679,-

Sample Size Calculations for Clustered and Longitudinal Outcomes in Clinical Research
729,-

Quantitative Drug Safety and Benefit Risk Evaluation
749,-

Clinical Trial Data Analysis Using R and SAS
1 729,-

Multiple Testing Problems in Pharmaceutical Statistics
679,-

Simultaneous Global New Drug Development
1 079,-

Real-World Evidence in Drug Development and Evaluation
729,-

Clinical Trial Optimization Using R
1 599,-

Handbook of Regression and Modeling
648,-

Design and Analysis of Bioavailability and Bioequivalence Studies
679,-

Methodologies in Biosimilar Product Development
679,-

Sample Size Calculations for Clustered and Longitudinal Outcomes in Clinical Research
729,-

Quantitative Drug Safety and Benefit Risk Evaluation
749,-

Clinical Trial Data Analysis Using R and SAS
1 729,-

Multiple Testing Problems in Pharmaceutical Statistics
679,-

Simultaneous Global New Drug Development
1 079,-

Real-World Evidence in Drug Development and Evaluation
729,-

Clinical Trial Optimization Using R
1 599,-

Handbook of Regression and Modeling
648,-