一共有10本书，都是最近几年出版的英文书。找得好辛苦，贴得也很累，希望大家多多回帖支持！！


（1） Formulation and Analytical Development for Low-Dose Oral Drug Products
By Jack Zheng.

Publisher: Wiley
Number Of Pages: 461
Publication Date: 2009-02-09
ISBN-10 / ASIN: 0470056096
ISBN-13 / EAN: 9780470056097
Product Description:
There are unique challenges in the formulation, manufacture, analytical chemistry, and regulatory requirements of low-dose drugs. This book provides an overview of this specialized field and combines formulation, analytical, and regulatory aspects of low-dose development into a single reference book. It describes analytical methodologies like dissolution testing, solid state NMR, Raman microscopy, and LC-MS and presents manufacturing techniques such as granulation, compaction, and compression. Complete with case studies and a discussion of regulatory requirements, this is a core reference for pharmaceutical scientists, regulators, and graduate students.

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（2）Technological Applications of Dispersions.
Publisher: CRC | ISBN: 0824791800 | edition 1994 | CHM | 576 pages | 4,42 mb

This comprehensive guide illustrates the effects of dispersions in applications, the means necessary to achieve these effects with optical results, and how to overcome or avoid the difficulties encountered;emphasizing the dispersions of solid particles in liquid or solid media. Providing insight into a wide range of well established and interrelated technologies, Technological Applications of Dispersions details the physical character of the disperse phase discusses major components of dispersions, including pigments explores surface coatings, optical effects, and recording of information explains strength enhancement of inorganic materials exemplifies emulsion polymerization, microencapsulation, and the control of crystal size, lattice type, and habit covers the stability and rheology of dispersions and the dispersibility of powders in liquids analyzes protein micelles in milk and the biological fate of drug carriers and more!

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（3）John Sharp - Good Pharmaceutical Manufacturing Practice: Rationale and Compliance.
Pages:288 | PDF | Interpharm Press Inc (30. Oktober 2004) | ISBN 0849319943 | 4.5 MB

Bridging the gap between U.S. regulations and European Good Manufacturing Practice guidelines, this book comparatively presents the major substance of both the U.S. Current Good Manufacturing Practice, parts 210 and 211 (US cGMPs) and the European Guide to Good Manufacturing Practice for Medicinal Products for Human and Veterinary Use (EU GMP guide). Based on the author's 40+ years experience, it offers special consideration of the reasoning behind the requirements, with specific regards to compliance methods. Topics also include personnel, documentation, premises and equipment, production, quality control, self-inspection, recalls, and more. This is an essential guidebook for those who wish to expand their pharmaceutical business in any international capacity.

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（4）Pharmaceutical Product Strategy.
Informa HealthCare; 1 edition | December 28, 2004 | ISBN: 0849327296 | 328 pages | PDF | 3.35 Mb

Borrowing time-tested Dynamic Modeling (DM) techniques from engineering, the authors illustrate the concept and resulting power of the DM methodology in pharmaceutical product development and brand management. The book examines issues surrounding utilization of information, consistency of assumptions, and the need for approaches that integrate the institutional knowledge of various functional areas as well as leverage the vast amount of secondary data available in the pharmaceutical industry. The authors detail how the DM approach facilitates the brand planning process in a systematic and accessible way. Issues of patient flow dynamics, physician adoption and prescribing patterns, as well as evaluation frameworks for specific treatment regimens are thoroughly examined. A later chapter details the extension of the DM framework to issues of pipeline portfolio.

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（5）


International Research in Healthcare.
Publisher: Pharmaceutical Press | Language: English | ISBN:0853697507 | 164 pages | Data: 2008 | PDF | 1 Mb

Description: This book is an essential guide for those thinking of undertaking a multi-centre research project. Research across international boundaries presents challenges with the need to consider relevance of research objectives and feasibility of procedures in different settings whilst maintaining scientific integrity in terms of design, instruments and execution.


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（6）Handbook of Industrial Mycology.
Publisher: CRC | ISBN: 082475655X | edition 2004 | PDF | 1159 pages | 11,6 mb

Several excellent books have been published that address one or more aspects of the diverse field of industrial mycology, but none of them cover the entire process of fungal bioactive metabolites discovery. Until now. The Handbook of Industrial Mycology provides, in one volume, an overview of recent developments in industrial mycology with emphasis on the discovery of bioactive metabolites and, most importantly, their underlying biology and genetics. Two additional features distinguish this book from other books in the field: 1) most chapters are prepared using experimental data to illustrate theories and 2) the authors provide methodologies and experimental protocols in their chapters. Presenting a comprehensive overview of recent advances, the book provides a framework of basic methods, tools, and organizational principles for channeling fungal germplasm into the academic, pharmaceutical, and enzyme discovery laboratories. It covers the complex range of processes involved in the discovery, characterization, and profiling of bioactive fungal metabolites. The book includes examples of several recently marketed fungal metabolites and explores the impact of fungi on applications in the pharmaceutical, food and beverage, agricultural, and agrochemical industries.

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（7）Enzyme Technologies for Pharmaceutical and Biotechnological Applications.
Publisher: Informa HealthCare | ISBN: 0824705491 | edition 2001 | PDF | 624 pages | 6,62 mb

Eli Lily and Company, Greenfield, ID. Reference providing an up-to-date review of enzyme functions in human and animal health, including coverage of new and emerging technologies in biotechnical and pharmaceutical industries. Emphasizes modern methods of metabolic engineering and drug discovery processes, and details enzymes related to human disease.

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Enzyme Technologies for Pharmaceutical and Biotechnological Applications.
Publisher: Informa HealthCare | ISBN: 0824705491 | edition 2001 | PDF | 624 pages | 6,62 mb

Eli Lily and Company, Greenfield, ID. Reference providing an up-to-date review of enzyme functions in human and animal health, including coverage of new and emerging technologies in biotechnical and pharmaceutical industries. Emphasizes modern methods of metabolic engineering and drug discovery processes, and details enzymes related to human disease.

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Enzyme Technologies for Pharmaceutical and Biotechnological Applications.
Publisher: Informa HealthCare | ISBN: 0824705491 | edition 2001 | PDF | 624 pages | 6,62 mb

Eli Lily and Company, Greenfield, ID. Reference providing an up-to-date review of enzyme functions in human and animal health, including coverage of new and emerging technologies in biotechnical and pharmaceutical industries. Emphasizes modern methods of metabolic engineering and drug discovery processes, and details enzymes related to human disease.

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（8）An Introduction to the U.S. Health Care System.
Publisher: Springer | Language: English | ISBN:082610214X | 328 pages | Data: 2007 | PDF | 13 Mb

Description: "Dr. Jonas has been a voice in the wilderness preaching sense about both health and health services for years. He clearly identifies the problems and issues facing the system and its beneficiaries, based upon the evidence he has carefully marshaled for the reader...and he challenges the reader to make sense out of the facts, understanding the evidence within a historical and international context, and come up with judgments on needed changes and how to go about making them, starting with the facts which he so generously provides you."--From the Foreword by Anthony R. Kovner, PhD Professor of Health Policy and Management New York University

This bestselling text is a concise and balanced classic presenting the domestic health care system. It explains the five major components of the U.S. health care system:

1. health care institutions (hospitals and nursing homes)
2. health care personnel (physicians, nurses, and others)
3. financing mechanisms
4. research and educational institutions that produce biomedical knowledge and health personnel
5. firms producing "health commodities" (such as pharmaceutical drugs and hospital equipment).

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（9）Impurities Evaluation of Pharmaceuticals.
Publisher: Informa HealthCare | ISBN: 0824798848 | edition 1998 | PDF | 304 pages | 11,74 mb

Filling a gap in the pharmaceutical literature, this unique guide addresses the development of targeted methodologies to monitor impurities in pharmaceutical compounds and drug products. Furnishes physicochemical protocols to determine the purity of pharmaceutical compounds fully before pharmacological and toxicological studies begin! Providing a clear definition of the subject, Impurities Evaluation of Pharmaceuticals introduces various techniques for isolating and characterizing impurities presents guidelines to evaluate stability using kinetic studies shows how to develop stability-indicating methodologies details various methods that require minimal sample prepreparation gives regulatory perspectives on chiral impurities and more! Containing important literature citations and offering an invaluable list of applications, Impurities Evaluation of Pharmaceuticals is an outstanding resource for pharmacists and pharmacologists clinical microbiologists, quality assurance and production managers in the pharmaceutical industry, analytical chemists and biochemists, pharmaceutical regulatory personnel, and upper-level undergraduate, graduate, and continuing-education students in these disciplines.

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（10）Jörg Knäblein "Modern Biopharmaceuticals: Design, Development and Optimization"
Wiley-VCH | 2005-12-06 | ISBN: 352731184X | Pages: 2022 | PDF | 24.94 MB

Due to the impressive accumulation of out-standing results, presented by brilliant, privileged and creative thinkers, this unique book reads like the ‘Who is Who’ of biotechnology. Never before has such an impressive group of individuals contributed to one biotechnology book, including Nobel Prize laureates Robert Huber, Thomas R. Cech, and Manfred Eigen as well as authors from the world's most famous academic institutes and biotech companies, such as ETH Zurich, MIT, Stanford, Yale, Princeton, Harvard Medical School, Max-Planck-Institute, Fraunhofer-Institute, Moscow Academy of Sciences, London Imperial College and Baxter, Invitrogen, MorphoSys, Roche, and Schering AG.

Modern Biopharmaceuticals is an essential reference work for biotechnologists, clinicians, medical doctors, pharmacists, pharmaceutical chemists, bio-chemists, molecular biologists, medicinal chemists, as well as all those working in the biotechnological and pharmaceutical industries, or medicinal institutes.

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