.- 1 Developability Assessment and Risk Management During Drug Discovery
.- 2 Discovery Formulations - Approaches and Practices in Early Preclinical Development
.- 3 Enabling Discovery Through Leveraging and Miniaturizing Pharmaceutical Principles and Processes
.- 4 Diagnosing Biopharmaceutical Limitations
.- 5 The Importance of Molecular Design Principles in Delivering High Quality Pharmaceutical Candidates
.- 6 Predictive Approaches to Establishing, Understanding, and Communicating Risk with Emphasis on Early Development
.- 7 Strategies and Methods for Drug Candidate Phase Optimization in Discovery Space
.- 8 Efficient Laboratory Methods to Assess Risk and Design Formulations
.- 9 Advanced X-ray Analytical Methods to Understand Structure, Properties and Risk
.- 10 Performance and Characterization of Amorphous Solid Dispersions: An Overview
.- 11 Hot-Melt Extrusion: The Process-Product-Performance Interplay
.- 12 Practical Considerations for Spray Dried Formulation and Process Development
.- 13 Nanosizing: "End-to-End" Formulation Strategy for Poorly-Water- Soluble Molecules
.- 14 Leveraging Solid State Form and Physiochemical Properties for Early Clinical Formulation Efforts: Opportunities and Challenges during Telcagepant Liquid Capsule Development.
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