Pharmaceutical Technology Products

  • Good Design Practices for GMP Pharmaceutical Facilities, Second Edition

    Edited by Terry Jacobs, Andrew A. Signore

    This revised publication serves as a handy and current reference for professionals engaged in planning, designing, building, validating and maintaining modern cGMP pharmaceutical manufacturing facilities in the U.S. and internationally. The new edition expands on facility planning, with a focus on…

    Hardback – 2016-06-27
    CRC Press
    Drugs and the Pharmaceutical Sciences

  • Nanotechnology and Drug Delivery, Volume Two

    Nano-Engineering Strategies and Nanomedicines against Severe Diseases

    Edited by Jose L. Arias

    The recent introduction of nanomedicines in the drug therapy arena is revolutionizing the management of severe diseases. The key advance in the field is the optimization of the biological fate of drug molecules, thus improving the therapeutic effect while keeping to a very minimum the associated…

    Hardback – 2016-02-25
    CRC Press

  • Bioreactors

    Animal Cell Culture Control for Bioprocess Engineering

    By Goutam Saha, Alok Barua, Satyabroto Sinha

    Bioreactors: Animal Cell Culture Control for Bioprocess Engineering presents the design, fabrication, and control of a new type of bioreactor meant especially for animal cell line culture. The new bioreactor, called the "see-saw bioreactor," is ideal for the growth of cells with a sensitive…

    Pack - Book & Ebook – 2015-12-18
    CRC Press

  • Fundamentals of Modern Bioprocessing

    By Sarfaraz K. Niazi, Justin L. Brown

    Biological drug and vaccine manufacturing has quickly become one of the highest-value fields of bioprocess engineering, and many bioprocess engineers are now finding job opportunities that have traditionally gone to chemical engineers. Fundamentals of Modern Bioprocessing addresses this growing…

    Hardback – 2015-11-04
    CRC Press

  • EU Annex 11 Guide to Computer Validation Compliance for the Worldwide Health Agency GMP

    By Orlando Lopez

    Good Manufacturing Practice (GMP) ensures medicinal products are produced consistently and controlled to the quality standards appropriate for their intended use and as required by product specifications or marketing authorization. Annex 11 details the European Medicines Agency (EMA) GMP…

    Hardback – 2015-04-06
    CRC Press

  • Introduction to Software for Chemical Engineers

    Edited by Mariano Martín Martín

    The field of chemical engineering is in constant evolution, and access to information technology is changing the way chemical engineering problems are addressed. Inspired by the need for a user-friendly chemical engineering text that demonstrates the real-world applicability of different computer…

    Hardback – 2014-07-01
    CRC Press

  • Biotechnology in Medical Sciences

    By Firdos Alam Khan

    As the field of medical biotechnology grows with new products and discoveries, so does the need for a holistic view of biotechnology in medicine. Biotechnology in Medical Sciences fulfills that need by delivering a detailed overview of medical biotechnology as it relates to human diseases and…

    Hardback – 2014-05-08
    CRC Press

  • Batch Processing

    Modeling and Design

    By Urmila Diwekar

    Although batch processing has existed for a long time, designing these processes and unit operations has been considered an onerous task that required computational efforts. Design of these processes is made more complex because of the time dependent nature of the process and the allowable…

    Hardback – 2014-02-25
    CRC Press

  • Advanced Aseptic Processing Technology

    Edited by James Agalloco, James Akers

    The preparation of sterile products using aseptic processing is considered perhaps the most critical process in the pharmaceutical industry and has witnessed continual improvement over the last half century. New approaches that have transformed classical aseptic production methods are appearing…

    Hardback – 2010-07-23
    CRC Press
    Drugs and the Pharmaceutical Sciences

  • Cleaning Validation Manual

    A Comprehensive Guide for the Pharmaceutical and Biotechnology Industries

    By Syed Imtiaz Haider

    During the past decades, enormous progress and enhancement of pharmaceutical manufacturing equipment and its use have been made. And while there are support documents, books, articles, and online resources available on the principles of cleaning and associated processing techniques, none of them…

    Hardback – 2010-05-24
    CRC Press

  • Pharmaceutical Computer Systems Validation

    Quality Assurance, Risk Management and Regulatory Compliance, 2nd Edition

    Edited by Guy Wingate

    Thoroughly revised to include the latest industry developments, the Second Edition presents a comprehensive overview of computer validation and verification principles and how to put them into practice. To provide the current best practice and guidance on identifying and implementing improvements…

    Hardback – 2010-02-23
    CRC Press

  • Pharmaceutical Process Engineering, Second Edition

    Edited by Anthony J. Hickey, David Ganderton

    With step-by-step methods of drug production and knowledge of major unit operations and key concepts of pharmaceutical engineering, this guide will help to improve communication among the varied professionals working in the pharmaceutical industry. Key features: REVISION OF A BESTSELLER - Updates…

    Hardback – 2009-10-22
    CRC Press
    Drugs and the Pharmaceutical Sciences

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