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Pharmaceutical Manufacturing Handbook: Production and Processes

ISBN: 978-0-470-25980-1

March 2008

1392 pages

Description
Everything you need to know to manufacture high-quality pharmaceuticals safely and efficiently

From the building of a facility to dosage and delivery forms to tablet production, this handbook covers the full range of topics to help you understand and apply the methods needed to manufacture drugs safely and efficiently. Thoroughly up to date, the handbook also examines the emerging role of nanotechnology in the development and manufacture of drugs and medical devices. Comprehensive in its presentation, this reference includes an entire section dedicated to the economics and business strategies of pharmaceutical manufacturing.

This handbook features contributions from a team of expert authors representing the manydisciplines within science, engineering, and technology that are involved in pharmaceutical manufacturing. They provide the information and tools you need to design, implement, operate,and troubleshoot a pharmaceutical manufacturing system. The editor, with more than thirty years' experience working with pharmaceutical and biotechnology companies, carefully reviewed all the chapters to ensure that each one is thorough, accurate, and clear.

Among the key topics covered are:

  • Radiopharmaceutical manufacturing

  • Clean facility design, construction, and maintenance

  • Controlled-release dosage forms

  • Biodegradable nanoparticles

  • Tablet production systems

  • Cyclodextrin-based nanomaterials in the pharmaceutical field

This publication serves as a hands-on reference for all scientists, engineers, and managers involved in pharmaceutical manufacturing, providing a basic primer for novices and detailing the latest discoveries and techniques for more experienced practitioners.

About the Author
SHAYNE COX GAD, PhD, DABT, ATS, is the Principal of Gad Consulting Services. Dr. Gad has more than thirty years of experience as a toxicologist, statistical consultant, manager, and general consultant on research and development in the chemical, consumer product, contract testing, biotechnology, medical device, and pharmaceutical industries. He is the author of twenty-nine books and numerous papers, presentations, and other publications.