1. INTRODUCTION

This general information chapter provides approaches for the development of dissolution test procedures for capsules, which are not provided by Dissolution 〈711〉, Drug Release 〈724〉, The Dissolution Procedure: Development and Validation 〈1092〉, and Disintegration and Dissolution of Dietary Supplements 〈2040〉. The chapter also discusses quality attributes associated with capsules that may affect the outcome of the dissolution testing.