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Showing 1 - 12 of 12 results for “randy jenkins”
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  • Audiobook

    Airbnb: How to Start and Grow a Profitable Airbnb Business Without Owning Property (The a-z Guide to Investing in Short-term Rentals and Generating Passive Income With Airbnb Business)

    by Randy Jenkins ...
    Narrated by Digital Voice Mason G ...

    Unabridged

    3 hours 17 min

    This audiobook is narrated by a digital voice.The Airbnb Passive Income Blueprint is a practical and inspiring guide that shows you exactly how to start and grow a profitable Airbnb business using rental arbitrage. Whether you're new to the idea of passive income or already exploring ways to earn more without trading time for money, this book offers a clear path forward. It breaks down what ... Read more

    $11.99 USD or Free with Kobo Plus

  • African Rhythms

    The Autobiography of Randy Weston

    by Randy Weston, Willard Jenkins, Ronald Radano, Josh Kun ...
    Series series a John Hope Franklin Center Book
    The pianist, composer, and bandleader Randy Weston is one of the world’s most influential jazz musicians and a remarkable storyteller whose career has spanned five continents and more than six decades. Packed with fascinating anecdotes, African Rhythms is Weston’s life story, as told by him to the music journalist Willard Jenkins. It encompasses Weston’s childhood in Brooklyn’s Bedford-Stuyvesant ... Read more

    $20.99 USD

  • FDA and Intellectual Property Strategies for Medical Device Technologies

    Including Artificial Intelligence, Software and Applications

    by 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 ...
    Series 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 ... Read more

    $116.99 USD

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  • Clinical Research Coordinator Handbook, 5th edition

    by Deborrah Norris ...
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  • Cobert's Manual of Drug Safety and Pharmacovigilance

    by Barton Cobert, William W Gregory, Jean-Loup Thomas ...
    Cobert's Manual of Drug Safety and Pharmacovigilance, Fourth Edition, is an updated how-to manual of guiding principles and concepts 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 ... Read more

    $48.99 USD

  • Supply Chain Management in the Drug Industry

    Delivering Patient Value for Pharmaceuticals and Biologics

    by 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 ... Read more

    $103.00 USD

  • The Combination Products Handbook

    A Practical Guide for Combination Products and Other Combined Use Systems

    Edited by 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 ... Read more

    $82.99 USD

  • The Survival Guide to EU Medical Device Regulations

    by 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 ... Read more

    $21.99 USD or Free with Kobo Plus

  • Risky Business: Sharing Health Data While Protecting Privacy

    Edited by 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 ... Read more

    $3.99 USD

  • Medical Device

    A Primer Based on Best Practices

    by 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 ... Read more

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  • The ASQ Certified Medical Device Auditor Handbook

    Edited by Scott A. Laman ...
    The ASQ Certified Medical Device Auditor Handbook (formerly The Biomedical Quality Auditor Handbook) was developed by the ASQ Medical Device Division (formerly Biomedical Division) in support of its mission to promote the awareness and use of quality principles, concepts, and technologies in the medical device community. It principally serves as a resource to candidates preparing for the Certified ... Read more

    $134.99 USD