Keeping pace with the latest technologies in the field, this guide describes the development of solid oral generic drug products from project initiation to market approval. Focusing on immediate-release and modified-release dosage forms, the book collects in-depth discussions from more than 30 noted
Process Simulation and Data Modeling in Solid Oral Drug Development and Manufacture
β Scribed by Marianthi G. Ierapetritou, Rohit Ramachandran (eds.)
- Publisher
- Humana Press
- Year
- 2016
- Tongue
- English
- Leaves
- 398
- Series
- Methods in Pharmacology and Toxicology
- Edition
- 1
- Category
- Library
No coin nor oath required. For personal study only.
β¦ Synopsis
This thorough volume aims to provide pharmaceutical engineers with an introduction to the current state of the art in modeling and simulation of pharmaceutical processes and to summarize a number of practical applications of relevant methodologies in drug product development. Chapters include explorations of simulation and modeling methodologies, data collection and analysis, development of novel sensing techniques, development and integration of individual unit models, optimization approaches for data-based models, design space evaluation techniques, informatics-based methodologies, and emerging topics in pharmaceutical process development. As a part of the Methods in Pharmacology and Toxicology series, the chapters contain the kind of detail and implementation advice that will make the transition into the laboratory as smooth as possible.
Authoritative and cutting edge, Process Simulation and Data Modeling in Solid Oral Drug Development and Manufacture seeks to promote research into process systems methodologies and their application in pharmaceutical product and process development, which will undoubtedly become an increasingly important area in the future.
β¦ Table of Contents
Front Matter....Pages i-x
Back Matter....Pages 1-42
....Pages 43-83
β¦ Subjects
Pharmacology/Toxicology
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