ABSTRACT

Emphasizing the role of good statistical practices (GSP) in drug research and formulation, this book outlines important statistics applications for each stage of pharmaceutical development to ensure the valid design, analysis, and assessment of drug products under investigation and establish the safety and efficacy of pharmaceutical compounds. Cove

chapter 1|25 pages

Introduction

chapter 2|21 pages

Pharmaceutical Validation

chapter 3|23 pages

Dissolution Testing

chapter 4|30 pages

Stability Analysis

chapter 5|43 pages

Bioavailability and Bioequivalence

chapter 6|20 pages

Randomization and Blinding

chapter 8|29 pages

Therapeutic Equivalence and Noninferiority

chapter 9|27 pages

Analysis of Incomplete Data

chapter 10|29 pages

Meta-Analysis

chapter 11|25 pages

Quality of Life

chapter 12|30 pages

Medical Imaging