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  • Handbook of Validation in Pharmaceutical Processes, Fourth Edition

    Revised to reflect significant advances in pharmaceutical production and regulatory expectations, Handbook of Validation in Pharmaceutical Processes, Fourth Edition examines and blueprints every step of the validation process needed to remain compliant and competitive. This book blends the use of theoretical knowledge with recent technological advancements to achieve applied practical solutions. ... Leer más

    $69.99 USD

  • Advanced Aseptic Processing Technology

    Edición de James Agalloco, James Akers ...
    Series 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 almost daily. This book reviews emerging technologies for aseptic processing that will markedly reduce ... Leer más

    $68.99 USD

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  • 3d Printing And Additive Manufacturing: Principles And Applications - Fifth Edition Of Rapid Prototyping

    Additive Manufacturing (AM) technologies are developing impressively and are expected to bring about the next revolution. AM is gradually replacing traditional manufacturing methods in some applications because of its unique properties of customisability and versatility. This book provides a very comprehensive and updated text about different types of AM technologies, their respective advantages, ... Leer más

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  • Rapid Prototyping: Principles And Applications (3rd Edition) (With Companion Cd-rom)

    Rapid prototyping (RP) has revolutionized how prototypes are made and small batch manufacturing is carried out. With rapid prototyping, the strategies used to produce a part change a number of important considerations and limitations previously faced by tool designers and engineers. Now in its third edition, this textbook is still the definitive text on RP. It covers the key RP processes, the ... Leer más

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  • Process Architecture in Biomanufacturing Facility Design

    Essential information for architects, designers, engineers, equipment suppliers, and other professionals who are working in or entering the biopharmaceutical manufacturing fieldBiomanufacturing facilities that are designed and built today are radically different than in the past. The vital information and knowledge needed to design and construct these increasingly sophisticated biopharmaceutical ... Leer más

    $160.00 USD

  • Good Design Practices for GMP Pharmaceutical Facilities

    Edición de Terry Jacobs ...
    Series series Drugs and the Pharmaceutical Sciences
    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 the ever-growing need to modify existing legacy facilities, and on current trends in pharmaceutical ... Leer más

    $70.99 USD

  • The Manufacture of Sterile Pharmaceuticals and Liquid Medical Devices Using Blow-Fill-Seal Technology

    Points to Consider

    This key document, produced by the BFS IOA, outlines important aspects on operation of BFS technology to ensure both compliance with cGMP regulations and the production of drug products of the appropriate quality, safety and efficacy. The Points to Consider document provides recommendations specific to the operation of Blow-Fill-Seal technology for the manufacture of sterile pharmaceuticals and ... Leer más

    $21.99 USD

  • Planning and Designing Research Animal Facilities

    Edición de Jack Hessler, Noel Lehner ...
    Series series American College of Laboratory Animal Medicine
    Research institutions have or are planning to build, expand and renovate animal research facilities to keep up with the demands of biomedical research caused in part by growth in the use of genetically altered rodents and the upsurge of research in infectious diseases. Properly designed facilities greatly facilitate effective management and high-quality day-to-day animal care that is required to ... Leer más

    $206.99 USD

  • Bioprocessing Piping and Equipment Design

    A Companion Guide for the ASME BPE Standard

    Series series Wiley-ASME Press Series
    The only comprehensive and authoritative reference guide to the ASME Bioprocessing Piping and Equipment (BPE) standardThis is a companion guide to the ASME Bioprocessing Piping and Equipment (BPE) Standard and explains what lies behind many of the requirements and recommendations within that industry standard. Following an introductory narrative to the Standard's early history, industry related ... Leer más

    $115.00 USD

  • Ultraviolet Disinfection for Wastewater

    Developed in conjunction with the International Ultraviolet Association, U ltraviolet Disinfection for Wastewater: Low-Dose Application Guidance for Secondary and Tertiary Discharges serves as a guide for consultants, wastewater utilities, and operators and provides introductory information on the advantages (and disadvantages) of UV disinfection compared to other commonly used technologies. It ... Leer más

    $129.99 USD o gratis con Kobo Plus

  • Biomedical Engineering and Design Handbook, Volume 2

    Volume 2: Biomedical Engineering Applications

    de Myer Kutz ...
    A State-of-the-Art Guide to Biomedical Engineering and Design Fundamentals and ApplicationsThe two-volume Biomedical Engineering and Design Handbook, Second Edition, offers unsurpassed coverage of the entire biomedical engineering field, including fundamental concepts, design and development processes, and applications. This landmark work contains contributions on a wide range of topics from ... Leer más

    $140.99 USD

  • Disposable Bioprocessing Systems

    Written by a researcher with experience designing, establishing, and validating biological manufacturing facilities worldwide, this is the first comprehensive introduction to disposable systems for biological drug manufacturing. It reviews the current state of the industry; tackles questions about safety, costs, regulations, and waste disposal; and guides readers to choose disposable components ... Leer más

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