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Books > Business & Economics > Industry & industrial studies > Manufacturing industries > Pharmaceutical industries

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Pharmaceutical Dosage Forms - Parenteral Medications - Volume 3: Regulations, Validation and the Future (Hardcover, 3rd edition) Loot Price: R4,975
Discovery Miles 49 750
Pharmaceutical Dosage Forms - Parenteral Medications - Volume 3: Regulations, Validation and the Future (Hardcover, 3rd...

Pharmaceutical Dosage Forms - Parenteral Medications - Volume 3: Regulations, Validation and the Future (Hardcover, 3rd edition)

Sandeep Nema, John D Ludwig

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Loot Price R4,975 Discovery Miles 49 750 | Repayment Terms: R466 pm x 12*

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This three-volume set of Pharmaceutical Dosage Forms: Parenteral Medications is an authoritative, comprehensive reference work on the formulation and manufacture of parenteral dosage forms, effectively balancing theoretical considerations with the practical aspects of their development. As such, it is recommended for scientists and engineers in the pharmaceutical industry and academia, and will also serve as an excellent reference and training tool for regulatory scientists and quality assurance professionals. First published in 1984 (as two volumes) and then last revised in 1993 (when it grew to three volumes), this latest revision will address the plethora of changes in the science and considerable advances in the technology associated with these products and routes of administration. The third edition of this book maintains the features that made the last edition so popular but comprises several brand new chapters, revisions to all other chapters, as well as high quality illustrations. Volume three presents: * An in-depth discussion of regulatory requirements, quality assurance, risk assessment and mitigation, and extractables/leachables. * Specific chapters on parenteral administrations devices, injection site pain assessment, and parenteral product specifications and stability testing. * Forward-thinking discussions on the future of parenteral product manufacturing, and siRNA delivery systems. * New chapters covering recent developments in the areas of visual inspection, quality by design (QbD), process analytical technology (PAT) and rapid microbiological methods (RMM ), and validation of drug product manufacturing process.

General

Imprint: Crc Press
Country of origin: United States
Release date: August 2010
First published: 2010
Editors: Sandeep Nema • John D Ludwig
Dimensions: 254 x 178 x 24mm (L x W x T)
Format: Hardcover - Cloth over boards
Pages: 326
Edition: 3rd edition
ISBN-13: 978-1-4200-8647-8
Categories: Books > Science & Mathematics > Biology, life sciences > General
Books > Professional & Technical > Technology: general issues > Engineering: general
Books > Professional & Technical > Environmental engineering & technology > General
Books > Business & Economics > Industry & industrial studies > Manufacturing industries > Pharmaceutical industries
Books > Professional & Technical > Industrial chemistry & manufacturing technologies > Industrial chemistry > Pharmaceutical technology
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LSN: 1-4200-8647-2
Barcode: 9781420086478

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