
eBook - ePub
Introduction to Pharmaceutical Technology Development
Journey from Lab to Shelf of Commercial Pharmaceutical Drugs
- 456 pages
- English
- ePUB (mobile friendly)
- Available on iOS & Android
eBook - ePub
Introduction to Pharmaceutical Technology Development
Journey from Lab to Shelf of Commercial Pharmaceutical Drugs
About this book
Introduction to Pharmaceutical Technology Development: Journey from Lab to Shelf of Commercial Pharmaceutical Drugs is a complete reference and learning resource for those working in pharmaceutics or aspiring to join the industry. The book provides a comprehensive view into all aspects of drug discovery, approval, and production. Using examples of well-known drugs and their journeys from lab to market, the book provides a comprehensive overview of all steps involved in bringing new drugs, including biologics, to the shelves.Topics covered include Drug Discovery, Pharmaceutical Formulations of Different Dose Form, Analytical Testing and Development, Unit Operations and Design for Major Equipment, Basics of Analytics and Process Validations and Protocols (DQ, IQ, OQ, PQ) in FDA-Regulated Industries.This book provides graduate students from several areas with a solid foundation of the Pharmaceutic industry across key stages on new drug lifecycle.
- Provides readers with introductory information on the developments in pharmaceutical technology
- Includes complete coverage of equipment and unit operations relevant across the production cycle of drugs
- Illustrates the path to commercialization through studies on the journey of several common commercially available formulated medications
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Information
Topic
MedicineSubtopic
OperationsTable of contents
- Title of Book
- Chapter 1. The modern-day drug discovery
- Chapter 2. Pharmaceutical product formulation of different dosage forms
- Chapter 3. Analytical testing and development in pharmaceutical technology
- Chapter 4. Unit operations and design for pharmaceuticals manufacturing and production
- Chapter 5. Basics of process validation and equipment qualification protocols (DQ, IQ, OQ, PQ) in FDA-regulated industries
- Chapter 6. Case studies in validation and protocols of pharmaceutical industry
- Chapter 7. Formulation, manufacturing and packaging of pharmaceutical dosage forms
- Chapter 8. Basics of biopharmaceuticals development, production, and quality
- Chapter 9. Key unit operations in biopharmaceuticals productions
- Chapter 10. Overview of good manufacturing practices (GMP)
- Chapter 11. Clinical research: Ethics & regulatory affair
- Chapter 12. Journey from lab to shelf: Omeprazole, Atorvastatin-Calcium, Acetazolamide, Allopurinol, Adacel
- Chapter 13. Journey from lab to shelf: Amoxicillin, Alprazolam, Penicillin, Acetaminophen, Metformin
- Index
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Yes, you can access Introduction to Pharmaceutical Technology Development by Yaser Dahman in PDF and/or ePUB format, as well as other popular books in Medicine & Operations. We have over 1.5 million books available in our catalogue for you to explore.