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FDA and Intellectual Property Strategies for Medical Device Technologies (Hardcover, 1st ed. 2019)
Loot Price: R4,054
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FDA and Intellectual Property Strategies for Medical Device Technologies (Hardcover, 1st ed. 2019)
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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 medical devices, as well as strategies for
successfully navigating the FDA regulatory review process.
Specifically, the first portion discusses the expansive range of
medical devices and then walks through the most common routes to
market: the PMA and 510(k) application processes. In the second
portion of this book, readers are introduced to the various types
of intellectual property rights that are available for medical
device technology inventions and innovations, and can explore ways
to overcome unique intellectual property challenges faced by many
medical device technology innovators. In the third portion of the
book, specific strategies are discussed to navigate the interface
between the FDA regulatory process and the process of obtaining
intellectual property protection. 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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