Pharmaceutical Laboratory Products

  • Pharmaceutical Master Validation Plan

    The Ultimate Guide to FDA, GMP, and GLP Compliance, 1st Edition

    By Syed Imtiaz Haider

    The Master Validation Plan provides a roadmap to management for on-time start-up of facility operations, and validation of existing facilities, in compliance with GMP requirements. The lack of a comprehensive Master Validation Plan and well-documented validation procedures is the main reason that…

    Hardback – 2001-12-27
    CRC Press

  • Containment in the Pharmaceutical Industry

    1st Edition

    By James P. Wood

    Delivering an encompassing overview of the factors, varieties, and applications determining product containment, this concise reference provides authoritative information on containment processes. It reviews the historical context, definition, evolution, and application of containment technology,…

    Hardback – 2000-09-25
    CRC Press
    Drugs and the Pharmaceutical Sciences

  • GLP Quality Audit Manual

    3rd Edition

    By Milton A. Anderson

    Designed to enable readers to plan and execute their own audits, this comprehensive guide presents both discussions and practical applications related to establishing a GLP QA unit and performing effective GLP audits. The first section provides the foundation of information needed for designing…

    Hardback – 2000-06-22
    CRC Press

  • Control of Particulate Matter Contamination in Healthcare Manufacturing

    1st Edition

    By Thomas A. Barber

    This book offers practical applications addressing the specifics of contamination, including particle origination, characterization, identification, and elimination, with a special focus on quality considerations. Written by an industry expert, this material offers a clear and concise understanding…

    Hardback – 1999-10-31
    CRC Press

  • International Stability Testing

    1st Edition

    Edited by David J. Mazzo

    In this book, recognized industry experts and regulatory inspectors from the world's pharmaceutical manufacturing regions provide stability requirements in all the major markets and discuss all aspects of stability testing and biotechnology. Participants in the ICH debates interpret the ICH…

    Hardback – 1998-08-31
    CRC Press

  • Clean Room Design

    Minimizing Contamination Through Proper Design, 1st Edition

    By Bengt Ljungqvist, Berit Reinmuller

    This practical book provides detailed guidance on all aspects of clean room airflow, the mechanics of airflow, and how microbial contamination is carried. Ljungqvist and Reinmüller draw on years of experience in clean room design and operation. The book contains maps of the effect of human…

    Hardback – 1996-11-30
    CRC Press

  • Last Rites

    The Work of the Modern Funeral Director, 1st Edition

    By Glennys Howarth

    Paperback – 1996-06-15
    Routledge

  • Automated Microbial Identification and Quantitation

    Technologies for the 2000s, 1st Edition

    Edited by Wayne P. Olson

    This book focuses on practical, proven applications to automate the microbial identification process economically and with greater levels of safety and quality for patients. A diverse group of recognized experts survey the topic and present the latest techniques and technologies for microbial…

    Hardback – 1996-01-31
    CRC Press

  • Laboratory Design Handbook

    1st Edition

    By E. Crawley Cooper

    Laboratory Design Handbook describes the process, motivation, constraints, challenges, opportunities, and specific design data related to the creation of a modern research laboratory. The information presented is based on a large pool of experience in the development of new and renovated laboratory…

    Hardback – 1994-05-05
    CRC Press

  • CRC Handbook of Chromatography

    Drugs, Volume III, 1st Edition

    By Ram N. Gupta

    These volumes provide a reference source of different gas chro-matographic, liquid chromatographic, or thin-layer chromatographic techniques for the qualitative determination of various therapeutic agents, including antibiotics, vitamins and hormones, drugs of abuse in body fluids, dosage forms, or…

    Hardback – 1988-12-31
    CRC Press
    Handbook of Chromatography

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