Overview
Investigates the FDA approval process as it pertains to medical device technology
Address some of the major FDA hurdles that medical device innovators often face while seeking approval
Discusses the interplay between FDA regulatory review of medical device technology and intellectual property strategy
Explores the benefits of protecting, managing and enforcing intellectual property obtained for medical device technology so that innovators can obtain the best possible commercial results from their IP ownership
Uses real case studies to illustrate concepts covered
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About this book
This book also includes a number of descriptive examples, case studies and scenarios to illustrate the topics discussed, and is intended for use by medical device designers, developers and innovators.
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Table of contents (17 chapters)
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FDA Strategies for Medical Device Technology
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Overview of Intellectual Property Rights for Medical Device Technology
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Implementation Strategies for Medical Device Innovators
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Authors and Affiliations
About the authors
Bibliographic Information
Book Title: FDA and Intellectual Property Strategies for Medical Device Technologies
Authors: Gerald B. Halt, John C. Donch, Amber R. Stiles, Lisa Jenkins VanLuvanee, Brandon R. Theiss, Dana L. Blue
DOI: https://doi.org/10.1007/978-3-030-04462-6
Publisher: Springer Cham
eBook Packages: Engineering, Engineering (R0)
Copyright Information: Springer Nature Switzerland AG 2019
Hardcover ISBN: 978-3-030-04461-9Published: 05 February 2019
eBook ISBN: 978-3-030-04462-6Published: 24 January 2019
Edition Number: 1
Number of Pages: XXIV, 333
Number of Illustrations: 30 b/w illustrations, 5 illustrations in colour
Topics: Biomedical Engineering and Bioengineering, Electronics and Microelectronics, Instrumentation, Engineering Economics, Organization, Logistics, Marketing