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1-12 sur 12 résultats pour « gerald b halt »
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  • FDA and Intellectual Property Strategies for Medical Device Technologies

    Including Artificial Intelligence, Software and Applications

    par Gerald B. Halt, Jr., John C. Donch, Jr., Amber R. Stiles, Brandon R. Theiss, Michelle Byrne, William F. Hodnick, Joshua Eldridge, Randy Goodman, Lisa Jenkins VanLuvanee, Dana L. Blue ...
    Collections series Engineering (R0)
    This book offers comprehensive, easy to understand guidance for medical device technology innovators on how to work through the United States Food and Drug Administration (US FDA) regulatory review and approval/grant/clearance process, while also providing insight on the various intellectual property concerns that many medical device innovators face. In the first portion of this book, readers are ... En savoir plus

    $153.99 CAD

  • FDA and Intellectual Property Strategies for Medical Device Technologies

    par Gerald B. Halt, John C. Donch, Amber R. Stiles, Lisa Jenkins VanLuvanee, Brandon R. Theiss, Dana L. Blue ...
    Collections series Engineering (R0)
    This book offers comprehensive, easy to understand guidance for medical device technology innovators on how to work through the United States FDA regulatory review process, while also providing insight on the various intellectual property concerns that many medical device innovators face. In the first portion of this book, readers are introduced to important concepts concerning FDA compliance for ... En savoir plus

    $153.99 CAD

  • Intellectual Property and Financing Strategies for Technology Startups

    par Gerald B. Halt, Jr., John C. Donch, Jr., Amber R. Stiles, Robert Fesnak ...
    Collections series Engineering (R0)
    This book offers a comprehensive, easy to understand guide for startup entities and developing companies, providing insight on the various sources of funding that are available, how these funding sources are useful at each stage of a company’s development, and offers a comprehensive intellectual property strategy that parallels each stage of development. The IP strategies offered in this book take ... En savoir plus

    $128.99 CAD

  • Intellectual Property in Consumer Electronics, Software and Technology Startups

    par Gerald B. Halt, Jr., Amber R. Stiles, John C. Donch, Jr., Robert Fesnak ...
    Collections series Engineering (R0)
    This book provides a comprehensive guide to procuring, utilizing and monetizing intellectual property rights, tailored for readers in the high-tech consumer electronics and software industries, as well as technology startups. Numerous, real examples, case studies and scenarios are incorporated throughout the book to illustrate the topics discussed. Readers will learn what to consider throughout ... En savoir plus

    $115.99 CAD

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  • Clinical Research Coordinator Handbook, Fourth Edition

    par Deborah Norris ...
    In this fully revised and expanded fourth edition of the essential reference for clinical research coordinators, Deborrah Norris provides expanded coverage of CRC duties and regulatory requirements, including new sections on investigator responsibilities, data clarification, and adverse event reporting. The books five appendices include a directory of CRC resources, updated forms and checklists, ... En savoir plus

    $9.61 CAD ou Gratuit avec Kobo Plus

  • Clinical Research Coordinator Handbook, 5th edition

    par Deborrah Norris ...
    “This extremely useful title is written for anyone planning to implement clinical trials at an institution. … the author has carefully detailed the types of forms, study records, and case report forms. … A powerful appendix and glossary of relevant terms help make this a needed book for any clinical trials office.”— Journal of Hospital LibrarianshipIn this fully revised and expanded fifth edition ... En savoir plus

    $13.73 CAD ou Gratuit avec Kobo Plus

  • Cobert's Manual Of Drug Safety And Pharmacovigilance (Third Edition)

    par Barton Cobert, William Gregory, Jean-loup Thomas ...
    Completely revised and updated, Cobert's Manual of Drug Safety and Pharmacovigilance, Third Edition, is a how-to manual for those working in the fields of drug safety, clinical research, pharmacology, regulatory affairs, risk management, quality/compliance, and in government and legal professions.This comprehensive and practical guide discusses the theory and the practicalities of drug safety ... En savoir plus

    $50.99 CAD

  • Supply Chain Management in the Drug Industry

    Delivering Patient Value for Pharmaceuticals and Biologics

    par Hedley Rees ...
    This book bridges the gap between practitioners of supply-chain management and pharmaceutical industry experts. It aims to help both these groups understand the different worlds they live in and how to jointly contribute to meaningful improvements in supply-chains within the globally important pharmaceutical sector. Scientific and technical staff must work closely with supply-chain practitioners ... En savoir plus

    $139.99 CAD

  • The Combination Products Handbook

    A Practical Guide for Combination Products and Other Combined Use Systems

    Modifié par Susan Neadle ...
    Combination products are therapeutic and diagnostic products that combine drugs, devices, and/or biological products. According to the US Food and Drug Administration (FDA), “a combination product is one composed of any combination of a drug and a device; a biological product and a device; a drug and a biological product; or a drug, device and a biological product.” Examples include prefilled ... En savoir plus

    $114.99 CAD

  • 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

    $132.99 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

  • Risky Business: Sharing Health Data While Protecting Privacy

    Modifié par Khaled El Emam ...
    Due to the digitization of medical records, more and more health data is readily available. This dynamic has created many opportunities to unlock this information and use it to improve medical practice, and through research and surveillance understand the effectiveness and side effects of drugs and medical devices to ultimately improve the public’s health. This data can also be used for commercial ... En savoir plus

    $5.99 CAD