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Pharmaceutical technology

Most popular at the top

  • Supercritical Fluid Technology for Drug Product Developmentby Peter York; Uday B. Kompella; Boris Y. Shekunov

    CRC Press 2004; US$ 179.95

    Interconnecting the fundamentals of supercritical fluid (SCF) technologies, their current and anticipated utility in drug delivery, and process engineering advances from related methodological domains and pharmaceutical applications, this volume unlocks the potential of supercritical fluids to further the development of improved pharmaceutical products-from... more...

  • 21 CFR Part 11by Orlando López

    CRC Press 2004; US$ 179.95

    Covering regulatory requirements stipulated by the FDA, this book delineates the organization, planning, verification, and documentation activities and procedural controls required for compliance with worldwide computer systems validation regulations. The author introduces supporting technologies such as encryption and digital signatures and places... more...

  • Management of Chemical and Biological Samples for Screening Applicationsby Mark Wigglesworth; Terry Wood

    Wiley 2012; US$ 200.00

    Mark Wigglesworth manages the UK Lead Optimization area of Sample Management Technologies for GlaxoSmith-Kline. Over the past 10 years Mark has managed large and small compound stores, assay ready plate production and compound set provision, as well as interacting with many areas of drug discovery. Additionally, he has led several drug discovery programs... more...

  • Drug Deliveryby Binghe Wang; Teruna J. Siahaan; Richard A. Soltero

    Wiley 2005; US$ 170.00

    BINGHE WANG, PhD, is a professor and Georgia Research Alliance Eminent Scholar in Drug Discovery, and Georgia Cancer Coalition Distinguished Cancer Scientist in the Department of Chemistry, Georgia State University. He is Editor in Chief of Medicinal Research Reviews and a member of the Long-Range Planning Committee of the American Chemical Society,... more...

  • Guide to Microbiological Control in Pharmaceuticals and Medical Devices, Second Editionby Stephen P. Denyer; Rosamund M. Baird

    Taylor and Francis 2006; US$ 210.00

    Microbiological matters continue to exercise considerable influence on product quality. In both the pharmaceutical and medical device industries, products of greater sophistication, along with evolving regulatory requirements, are elevating the challenges related to maintaining microbiological integrity. Updated to reflect technological and regulatory... more...

  • Lipospheres in Drug Targets and Deliveryby Claudio Nastruzzi

    Taylor and Francis 2004; US$ 262.00

    Lipospheres in Drug Targets and Delivery: Approaches, Methods, and Applications presents an overview of the most recent applications of lipospheres primarily in the field of medicine, pharmaceutics, and biotechnology. It includes chapters on preparation, characterization, delivery (of peptides, proteins, vaccines, nucleic acids), therapeutic applications... more...

  • Isolation Technologyby Tim Coles

    Taylor and Francis 2004; US$ 304.00

    The most significant changes in isolation technology during the past five years have not been in the technology itself but in its increased acceptance. This acceptance is clearly demonstrated by the series of monographs, guidelines, and standards produced by regulatory bodies to describe best practice in the design and operation of isolators. Thoroughly... more...

  • Microbiological Contamination Control in Pharmaceutical Clean Roomsby Nigel Halls

    Taylor and Francis 2004; US$ 304.00

    Contamination control in pharmaceutical clean rooms has developed from a jumble of science and engineering, knowledge of what has worked well or badly in the past, dependent upon the technology available at the time the clean room was built and subsequent technological developments. Surrounding it all is a blanket of regulations. Taking a multidisciplinary... more...

  • Quality by Kate McCormick

    Elsevier Science 2002; US$ 310.00

    The Pharmaceutical Engineering Series is a comprehensive reference for the pharmaceutical professional covering all aspects from quality, documentation and validation through manufacturing processes to facility design and management. In 'Quality', Dr Kate McCormick provides the reader with comprehensive coverage of this vital subject, including the... more...

  • Six Sigma in the Pharmaceutical Industryby Brian K. Nunnally; John S. McConnell

    Taylor and Francis 2007; US$ 115.95

    The pharmaceutical industry is under increasing pressure to do more with less . Drug discovery, development, and clinical trial costs remain high and are subject to rampant inflation. Ever greater regulatory compliance forces manufacturing costs to rise despite social demands for more affordable health care. Traditional methodologies are failing... more...