| Introduction and Overview | |
| Preliminary Preformulation | |
| Accelerating the Course of Preliminary-Preformulation through Prediction of Molecular Physical Properties and Integrated Analytical Data Management s | |
| Prediction of Crystallographic Characteristics | |
| Salt Selection for Pharmaceutical Compounds | |
| Intelligent Preformulation Design and Predictions using Artificial Neural Networks | |
| Profiling the Drug Substance | |
| Developing a Profile of the Active Pharmaceutical Ingredient | |
| Particle Morphology and Characterization in Preformulation | |
| Preparation and Identification of Polymorphs and Solvatomorphs | |
| X-Ray Diffraction Methods for the Characterization of Solid Pharmaceutical Materials | |
| Spectroscopic Methods for the Characterization of Drug Substances | |
| Thermal Analysis and Calorimetric Methods for the Characterization of New Crystal Forms | |
| Solubility Methods for the Characterization of New Crystal Forms | |
| Development of the Ideal Formulation | |
| Overview of the Solid Dosage Form Preformulation Program | |
| Drug-Excipient Interactions Appropriate to Solid Dosage Forms | |
| Methods for the Determination of the Physical and Chemical Stability of a New Solid Dosage Form | |
| Dissolution Testing | |
| Beyond Preformulation | |
| Structure (Content, Format of the Preformulation Report | |
| Significance of Drug Substance Physicochemical Properties in Regulatory Quality by Design | |
| Table of Contents provided by Publisher. All Rights Reserved. |
Preformulation in Solid Dosage Form Development
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