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« wolfgang ecker »

1-12 sur 12 résultats pour « wolfgang ecker »
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  • Medical Devices and IVDs

    Fit for the new EU-Regulations: Your complete seminar for projekt, study and job

    par Wolfgang Ecker ...
    With this book, you get a really complete seminar for the new Regulations on medical devices and IVDs in the EU, ready at hand, at any time. These EU regulations create new rules for medical technology and laboratory diagnostics in Europe. Concise regulatory know-how is now required to keep or reposition medical devices and in vitro diagnostics on the European market, from syringes, contact lenses ... En savoir plus

    $40.99 CAD ou Gratuit avec Kobo Plus

  • Clinical Evaluation and Investigation of Medical Devices under the new EU-Regulation

    par Wolfgang Ecker, Gerold Labek, Tarquin Mittermayr, Brigitte Raffeiner, Michael Ring, Bernhard Schwartz ...
    "The concept of clinical evaluation and the framework for clinical investigations have been significantly enforced within the new EU-Medical Device Regulation (MDR). This book provides in-depth and practice-oriented guidance on the systematic identification and generation of clinical data through clinical investigations and other relevant sources. It addresses the needs of all stakeholders, be it ... En savoir plus

    $44.99 CAD ou Gratuit avec Kobo Plus

  • Medizinprodukte und IVD

    Die neuen EU-Verordnungen Ihr Komplettseminar für Projekt, Studium und Beruf

    par Wolfgang Ecker ...
    Sie bekommen mit diesem Buch ein echtes Komplett-Seminar für den Bereich Medizinprodukte und IVD in der EU jederzeit griffbereit in die Hand. Das Buch gibt Ihnen gleich einen raschen, verlässlichen Überblick über diese neue EU-Materie. Sie ersparen sich damit unzählige Seminare, ob in Präsenz oder, oft nicht minder anstrengend, online. Alle wichtigen Aspekte werden gründlich aufbereitet. Sie ... En savoir plus

    $47.99 CAD

  • Medizinprodukte und IVD

    Die neuen EU-Verordnungen Ihr Komplettseminar für Projekt, Studium und Beruf

    par Wolfgang Ecker ...
    Sie bekommen mit diesem Buch ein echtes Komplettseminar für den Bereich Medizinprodukte und IVD in der EU jederzeit griffbereit in die Hand. Das Buch gibt Ihnen gleich einen raschen, verlässlichen Überblick über diese neue, oft als schwierig empfundene EU-Materie. Sie ersparen sich damit unzählige Seminare, ob in Präsenz oder, oft nicht minder anstrengend, online. Alle wichtigen Aspekte werden ... En savoir plus

    $46.99 CAD

  • Medizinprodukte und IVD

    Fit für Europa

    par Wolfgang Ecker, Andreas Aichinger ...
    Die EU-Verordnungen zu Medizinprodukten und IVD schaffen neue Spielregeln für die Medizintechnik und Labordiagnostik in Europa. Prägnantes regulatorisches Know-how ist jetzt gefragt, um Medizinprodukte und In-vitro-Diagnostika auf dem europäischen Markt zu halten oder dort neu zu platzieren. Die richtige regulatorische Strategie einer Organisation kann im Hinblick auf Compliance, Time to Market ... En savoir plus

    $74.99 CAD

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  • Health Informatics: Practical Guide, Seventh Edition

    par Robert E. Hoyt, William R. Hersh ...
    Health Informatics: Practical Guide focuses on the application of information technology in healthcare to improve individual and population health, education and research. The goal of the seventh edition is to stimulate and educate healthcare and IT professionals and students about the key topics in this rapidly changing field. Dr. William Hersh from Oregon Health & Science University is the co ... En savoir plus

    $41.99 CAD

  • Medical Product Regulatory Affairs

    Pharmaceuticals, Diagnostics, Medical Devices

    par John J. Tobin, Gary Walsh ...
    Written in a clear and concise style by an experienced author, this attractively-priced book covers regulatory affairs in all major global markets for pharmaceuticals and medical devices, making it the most comprehensive in its field.Following a look at drug development, complete sections are devoted to national and EU regulatory issues, manufacturing license application and retention, and ... En savoir plus

    $116.99 CAD

  • Leveraging Data Science for Global Health

    Modifié par Leo Anthony Celi, Maimuna S. Majumder, Patricia Ordóñez, Juan Sebastian Osorio, Kenneth E. Paik, Melek Somai ...
    This open access book explores ways to leverage information technology and machine learning to combat disease and promote health, especially in resource-constrained settings. It focuses on digital disease surveillance through the application of machine learning to non-traditional data sources. Developing countries are uniquely prone to large-scale emerging infectious disease outbreaks due to ... En savoir plus

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  • 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

  • Process Mining in Healthcare

    Evaluating and Exploiting Operational Healthcare Processes

    par Rob J. B. Vanwersch, Ronny S. Mans, Wil M. P. van der Aalst ...
    Collections series Computer Science (R0)
    What are the possibilities for process mining in hospitals? In this book the authors provide an answer to this question by presenting a healthcare reference model that outlines all the different classes of data that are potentially available for process mining in healthcare and the relationships between them. Subsequently, based on this reference model, they explain the application opportunities ... En savoir plus

    $83.99 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

  • 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