Medical Technology Development and Commercialization (Classic Reprint)
Language: English
Published by Forgotten Books, 2018
- Softcover
- New



Seller: Forgotten Books, London, United KingdomForgotten Books
AbeBooks seller since June 2, 2021
Condition: New
US$ 19.36
Quantity: Over 20 available
Add to basketItem description from seller
Print on Demand. This book delves into the impact of government policies on the development and commercialization of medical technologies in the United States. The author draws on firsthand accounts from industry leaders to highlight the challenges faced by companies seeking to bring new and innovative medical devices and drugs to market. The book explores the delicate balance between ensuring public safety and fostering innovation, examining the effectiveness of existing regulations and the need for reform. It discusses the impact of policies on clinical trials, research and development, and manufacturing, raising concerns about the potential loss of U.S. leadership in medical technology and the implications for patients' access to life-saving treatments. Ultimately, the book underscores the significance of addressing these challenges to ensure continued advancements in medical technology and improve healthcare outcomes for all. This book is a reproduction of an important historical work, digitally reconstructed using state-of-the-art technology to preserve the original format. In rare cases, an imperfection in the original, such as a blemish or missing page, may be replicated in the book.…
Seller Inventory # 9781331234982_0
- Title
- Medical Technology Development and Commercialization (Classic Reprint)
- Author
- Unknown Author
- Publisher
- Forgotten Books
- Publication year
- 2018
- Condition
- New
- Book Type
- print-on-demand item
- Binding
- Paperback
- Language
- English
- ISBN 10
- 1331234980
- ISBN 13
- 9781331234982
- Seller catalogs
- General Administrative Records
How government rules shape the future of medical technology—and what it means for faster, safer access to new devices and drugs.
This book compiles a detailed look at how tax policies, regulatory oversight, and other laws impact the development and commercialization of medical technologies. It examines why timely innovation matters for patients and for the U.S. economy, and it discusses the tradeoffs between safety, efficacy, and speed to market. The text covers perspectives from lawmakers, industry leaders, and regulators, highlighting ongoing debates about how to reform the regulatory environment without compromising public health.
- Learn how regulatory policy has evolved and what it means for new devices and therapies.
- Understand the roles of the FDA and international counterparts in device review, postmarket surveillance, and safety standards.
- See arguments for and against different reform approaches, including efficiency, cost, and patient outcomes.
- Explore scenarios where policy changes could accelerate innovation while maintaining patient safety.
"Synopsis" may belong to another edition of this title.
Forgotten Books
London, United Kingdom
AbeBooks seller since June 2, 2021
Shipping rates from United Kingdom to U.S.A.
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Store description
Forgotten Books’ Classic Reprint Series utilizes the latest technology to regenerate facsimiles of historically important writings. Careful attention has been made to accurately preserve the original format of each page whilst digitally enhancing the quality of the aged text.
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FB &c Ltd
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All books are Print on Demand and will be printed upon purchase and shipped in New Condition. Orders typically ship within 3-5 business days. If you're dissatisfied with your purchase (Incorrect Book/Not as Described/Damaged) or if the order hasn't arrived, you're eligible for a refund within 30 days of the estimated delivery date. If you've changed your mind about a book that you've ordered, please use the ask bookseller a question link to contact us and we'll respond within 2 business days.
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