Author: Elaine Whitmore
Edition: 2
Binding: Paperback
ISBN: 0873896130
Edition: 2
Binding: Paperback
ISBN: 0873896130
Development of FDA-Regulated Medical Products: Prescription Drugs, Biologics, and Medical Devices
There have been revolutionary changes to the classification and regulation of prescription drugs, biologics, and medical devices since the previous edition of this book was published in 1997 under the title Product Development Planning for Health Care Products Regulated by the FDA. The revised book includes: a review of the significant changes within the FDA that affect the requirements and review of medical products; updated facts and figures; expansion of subjects that have grown more critical, such as clinical outcomes, human factors, and marketing objectives; and additional new topics such as the role of product development in hazard analysis, recalls, and product liability. This book is intended as a foundation for anyone involved in product 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
This book is intended as a foundation for anyone involved in product
