Author: Elaine Whitmore
Edition: 2
Binding: Hardcover
ISBN: 0873898338
Edition: 2
Binding: Hardcover
ISBN: 0873898338
Development of FDA-Regulated Medical Products: A Translational Approach, Second Edition
Translating promising discoveries and innovations into useful, marketable medical products demands a robust process to guide nascent products through a tangle of scientific, clinical, regulatory, economic, social, and legal challenges. There are so many human and environmental elements involved in shepherding medical advances from lab to launch that the field of medical product development has been referred to as an ecosystem. The purpose of this book is to help provide a shared foundation from which cross-functional participants in that ecosystem can negotiate the product development labyrinth and accomplish the goal of providing both groundbreaking and iterative new medical products. The book is intended for anyone in industry, the public Development of FDA-Regulated Medical Products Read medical textbooks online like Development of FDA-Regulated Medical Products here
Development of FDA-Regulated Medical Products: A Translational Approac
Development of FDA Regulated Medical Products covers Food and Drug Administrations Modernization Act (FDAMA), along with discussions on Intellectual Property, Pharmacoeconomics, and Technological and Medical Trends. Intended for those interested in medical product development.
Development of FDA-Regulated Medical Products : A Translational Approach, ISBN-13: 9780873898331, ISBN-10: 0873898338
Powered by Frooition Pro Click here to view full size. Full Size Image Click to close full size. Development of Fda-Regulated Medical Products [9780873896139] - Book NEW Author(s): Elaine Whitmore Format: Paperback # Pages: 202 ISBN-13: 9780873896139 Published: 12/01/2003 Language: English Weight: 1.10 pounds Brand new book. About Us Payment Shipping Customer Service FAQs Welcome to MovieMars All items are Brand New. We offer unbeatable prices, quick shipping times and a wide selection second t
Translating promising discoveries and innovations into useful, marketable medical products demands a robust process to guide nascent products through a tangle of scientific, clinical, regulatory, economic, social, and legal challenges. There are so many human and environmental elements involved in shepherding medical advances from lab to launch that the field of medical product development has been referred to as an ecosystem.The purpose of this book is to help provide a shared foundation from
Development of FDA-Regulated Medical Products Online
There are so many human and environmental elements involved in shepherding medical advances from lab to launch that the field of medical product development has been referred to as an ecosystem
The book is intended for anyone in industry, the public
