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Pharmaceutical Technology Books

You are currently browsing 1–10 of 47 new and published books in the subject of Pharmaceutical Technology — sorted by publish date from newer books to older books.

For books that are not yet published; please browse forthcoming books.

New and Published Books

  1. 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...

    Published April 6th 2015 by CRC Press

  2. 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...

    Published July 1st 2014 by CRC Press

  3. 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...

    Published May 8th 2014 by CRC Press

  4. 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...

    Published February 25th 2014 by CRC Press

  5. Advanced Aseptic Processing Technology

    Edited by James Agalloco, James Akers

    Series: Drugs and the Pharmaceutical Sciences

    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...

    Published July 23rd 2010 by CRC Press

  6. Cleaning Validation Manual

    A Comprehensive Guide for the Pharmaceutical and Biotechnology Industries

    By Syed Imtiaz Haider, Syed Erfan Asif

    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...

    Published May 24th 2010 by CRC Press

  7. 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...

    Published February 23rd 2010 by CRC Press

  8. Pharmaceutical Process Engineering, Second Edition

    Edited by Anthony J. Hickey, David Ganderton

    Series: Drugs and the Pharmaceutical Sciences

    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...

    Published October 22nd 2009 by CRC Press

  9. Design and Analysis of Bioavailability and Bioequivalence Studies, Third Edition BABE-Solution bundle version

    Edited by Shein-Chung Chow, Jen-pei Liu

    Series: Chapman & Hall/CRC Biostatistics Series

    Containing four new chapters, along with several new and updated sections, this third edition reviews the latest progress of activities and results in bioavailability and bioequivalence on regulatory requirements, scientific and practical issues, and statistical methodology. It presents the current...

    Published March 23rd 2009 by CRC Press

  10. Sample Size Calculations in Clinical Research, Second Edition N-Solution bundle version

    Edited by Shein-Chung Chow, Jun Shao

    Series: Chapman & Hall/CRC Biostatistics Series

    This book explains how the formulas and procedures for sample size calculations can be used in a variety of clinical research and development stages. It presents real-world examples from several therapeutic areas and explores emerging topics in pharmaceutical research and development. This edition...

    Published March 23rd 2009 by Chapman and Hall/CRC