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Meilleures séries dans ce pays : Canada

1-12 sur 12 résultats pour « maja ravnikar »
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  • Molecular Methods in Plant Disease Diagnostics

    Principles and Protocols

    par James Woodhall, Ian Adams, Rachel Glover, Susan Seal, Bart van de Vossenberg, Maja Ravnikar, Adrian Fox, Jennifer Hodgetts, Juerg Frey ...
    Using molecular methods for plant disease diagnosis provides diagnosticians with a number of advantages over more traditional methods. They can allow the identification of morphologically similar species, for example, or the detection of infection prior to symptom formation. Not only can molecular tools help by increasing the efficacy, accuracy and speed of diagnosis; their common technological ... En savoir plus

    $134.99 CAD

  • Critical Points for the Organisation of Test Performance Studies in Microbiology

    Plant Pathogens as a Case Study

    Modifié par Ana Vučurović, Nataša Mehle, Géraldine Anthoine, Tanja Dreo, Maja Ravnikar ...
    Collections Livre 12 - Plant Pathology in the 21st Century
    This open access book in the field of plant pest detection shows a constant demand in development and improvement of fast and reliable detection tools, especially for high-priority pests. This open access book describes and summarizes the whole process of the organization of test performance study (TPS) for these tools. The outcome of TPS, obtained through the evaluation of the performance of one ... En savoir plus

    Gratuit

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  • Clinical Governance: Improving The Quality Of Healthcare For Patients And Service Users

    par Mary Gottwald, Gail Lansdown ...
    This is an accessible and practical guide to clinical governance in healthcare, designed to help practitioners and students deliver better care to patients. ... En savoir plus

    $51.99 CAD

  • Health informatics

    Improving patient care

    Modifié par BCS, The Chartered Institute for IT ...
    Health informatics (HI) and technology play a major role in health care including empowering patients, shortening waiting lists and improving treatment efficiency. This ebook contains a range of material by HI experts on the latest developments. It includes articles on robotic surgery, on how technology can support people in their own homes, and on how electronic systems can help reduce risk of ... En savoir plus

    $4.99 CAD

  • How to Succeed at the Medical Interview

    par Chris Smith, Darryl Meeking ...
    Collections Livre 42 - How To
    How to Succeed at the Medical Interview provides candidates with a competitive edge. It reduces the likelihood of unexpected questions or situations and helps improve confidence before and during the medical interview.This new second edition includes updated content on changes to the structure of healthcare and how this affects both the application and interview process. It details the types of ... En savoir plus

    $42.99 CAD

  • How To Write a Paper

    Modifié par George M. Hall ...
    Collections series How To
    This concise paperback is one of the best known guides to writing a paper for publication in biomedical journals. Its straightforward format – a chapter covering each of part of the structured abstract – makes it relevant and easy to use for any novice paper writer.How to Write a Paper addresses the mechanics of submission, including electronic submission, and how publishers handle papers, writing ... En savoir plus

    $46.99 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

  • 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

  • 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 Validation in Pharmaceutical Processes, Fourth Edition

    Modifié par James Agalloco, Phil DeSantis, Anthony Grilli, Anthony Pavell ...
    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. ... En savoir plus

    $96.99 CAD

  • Design Controls for the Medical Device Industry, Third Edition

    par Marie B. Teixeira ...
    This third edition provides a substantial comprehensive review of the latest design control requirements, as well as proven tools and techniques to ensure a company's design control program evolves in accordance with current industry practice. It assists in the development of an effective design control program that not only satisfies the US FDA Quality Systems Regulation (QSR) and 13485:2016 ... En savoir plus

    $336.99 CAD

  • A Comprehensive and Practical Guide to Clinical Trials

    Modifié par Brenda Wright, Delva Shamley ...
    A Comprehensive and Practical Guide to Clinical Trials provides an overview of the entire process of clinical research in one thorough and easy-to-read handbook that offers those involved in clinical research a clear understanding of how the components of a study are related. It focuses on the practical aspects of the preparation and execution of a clinical trial and offers tools and resources to ... En savoir plus

    $79.99 CAD