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Reference Module Computer Science and Engineering Série de Livres électroniques

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  • Medical Devices and In Vitro Diagnostics

    Requirements in Europe

    Modifié par Christian Baumgartner, Johann Harer, Jörg Schröttner ...
    Collections series Reference Module Computer Science and Engineering
    This updatable reference work gives a comprehensive overview of all relevant regulatory information and requirements for manufacturers and distributors around medical and in-vitro diagnostic devices in Europe. These individual requirements are presented in a practice-oriented manner, providing the reader with a concrete guide to implementation with main focus on the EU medical device regulations, ... En savoir plus

    $513.99 CAD

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  • Logistics Operations and Management

    Concepts and Models

    Modifié par Reza Farahani, Shabnam Rezapour, Laleh Kardar ...
    This book provides a comprehensive overview of how to strategically manage the movement and storage of products or materials from any point in the manufacturing process to customer fulfillment. Topics covered include important tools for strategic decision making, transport, packaging, warehousing, retailing, customer services and future trends. - An introduction to logistics - Provides practical ... En savoir plus

    $132.79 CAD

  • Clinical Engineering Handbook

    Modifié par Joseph Dyro ...
    As the biomedical engineering field expands throughout the world, clinical engineers play an evermore-important role as translators between the medical, engineering, and business professions. They influence procedure and policy at research facilities, universities, as well as private and government agencies including the Food and Drug Administration and the World Health Organization. The ... En savoir plus

    $167.99 CAD

  • Industry 4.0: Managing The Digital Transformation

    par Alp Ustundag, Emre Cevikcan ...
    Collections series Engineering (R0)
    This book provides a comprehensive guide to Industry 4.0 applications, not only introducing implementation aspects but also proposing a conceptual framework with respect to the design principles. In addition, it discusses the effects of Industry 4.0, which are reflected in new business models and workforce transformation. The book then examines the key technological advances that form the pillars ... En savoir plus

    $294.99 CAD

  • Medical Device

    A Primer Based on Best Practices

    par Rommel Garcia ...
    This book is meant to be a guide to all who want to learn about a highly regulated industry. My approach is to give you, the reader, an example of a fictitious device, and we will take it from a conceptual idea all the way to launch and beyond. My intention is to incorporate the best experiences that I and other contributors have had into this book and convert them into laymans terms for those who ... En savoir plus

    $5.99 CAD

  • How to Validate a Pharmaceutical Process

    par Steven Ostrove ...
    Collections series Expertise in Pharmaceutical Process Technology
    How to Validate a Pharmaceutical Process provides a "how to approach to developing and implementing a sustainable pharmaceutical process validation program. The latest volume in the Expertise in Pharmaceutical Process Technology Series, this book illustrates the methods and reasoning behind processes and protocols. It also addresses practical problems and offers solutions to qualify and validate a ... En savoir plus

    $44.79 CAD

  • The Survival Guide to EU Medical Device Regulations

    par Petri Pommelin ...
    The Regulations for medical devices and in vitro diagnostic medical devices were published in the Official Journal of the European Union on 5 May 2017, and they entered into force 26 May 2017. A regulation is a legal act of the European Union that becomes immediately enforceable as law in all Member States simultaneously. This book gives guidance on the definitions, the key concepts and the main ... En savoir plus

    $28.99 CAD ou Gratuit avec Kobo Plus

  • Nursing Informatics for the Advanced Practice Nurse, Second Edition

    Patient Safety, Quality, Outcomes, and Interprofessionalism

    par Susan McBride, PhD, RN-BC, CPHIMS, FAAN, Mari Tietze, PhD, RN, FHIMSS, FAAN ...
    A “must have” text for all healthcare professionals practicing in the digital age of healthcare.Nursing Informatics for the Advanced Practice Nurse, Second Edition, delivers a practical array of tools and information to show how advanced practice nurses can maximize patient safety, quality of care, and cost savings through the use of technology. Since the first edition of this text, health ... En savoir plus

    $155.99 CAD

  • CAPA in the Pharmaceutical and Biotech Industries

    How to Implement an Effective Nine Step Program

    par J Rodriguez ...
    Collections series Woodhead Publishing Series in Biomedicine
    CAPA in the Pharmaceutical and Biotech Industries: How to Implement an Effective Nine Step Program contains the most current information on how to implement, develop, and maintain an effective Corrective Action and Preventive Action (CAPA) and investigation program using a nine step closed-loop process approach for medical devices and pharmaceutical and biologic manufacturers, as well as any ... En savoir plus

    $181.59 CAD

  • Risk Management Applications in Pharmaceutical and Biopharmaceutical Manufacturing

    Modifié par Hamid Mollah, Harold Baseman, Mike Long ...
    Collections Livre 4 - Wiley Series in Biotechnology and Bioengineering
    Sets forth tested and proven risk management practices in drug manufacturingRisk management is essential for safe and efficient pharmaceutical and biopharmaceutical manufacturing, control, and distribution. With this book as their guide, readers involved in all facets of drug manufacturing have a single, expertly written, and organized resource to guide them through all facets of risk management ... En savoir plus

    $163.99 CAD

  • Handbook of Medical Device Regulatory Affairs in Asia

    Second Edition

    Modifié par Jack Wong, Raymond Tong ...
    Medical device regulation in Asia has gained more importance than ever. Governments and regulatory bodies across the region have put in place new regulatory systems or refined the existing ones. A registered product requires a lot of technical documentation to prove its efficacy, safety, and quality. A smooth and successful registration process demands soft skills for dealing with various key ... En savoir plus

    $211.99 CAD

  • Advanced Product Quality Planning

    The Road to Success

    par D. H. Stamatis ...
    Collections series Practical Quality of the Future
    This book defines, develops, and examines the foundations of the APQP (Advanced Product Quality Planning) methodology. It explains in detail the five phases, and it relates its significance to national, international, and customer specific standards. It also includes additional information on the PPAP (Production Part Approval Process), Risk, Warranty, GD&T (Geometric Dimensioning and Tolerancing) ... En savoir plus

    $102.99 CAD