Re-Engineering Clinical Trials - Best Practices for Streamlining the Development Process (Hardcover, UK ed.)

The pharmaceutical industry is currently operating under a business model that is not sustainable for the future. Given the high costs associated with drug development, there is a vital need to reform this process in order to provide safe and effective drugs while still securing a profit. Re-Engineering Clinical Trials evaluates the trends and challenges associated with the current drug development process and presents solutions that integrate the use of modern communication technologies, innovations and novel enrichment designs. This book focuses on the need to simplify drug development and offers you well-established methodologies and best practices based on real-world experiences from expert authors across industry and academia. Written for all those involved in clinical research, development and clinical trial design, this book provides a unique and valuable resource for streamlining the process, containing costs and increasing drug safety and effectiveness.

General

Imprint:	Academic Press Inc
Country of origin:	United States
Release date:	December 2014
First published:	2015
Editors:	Peter Schueler • Brendan Buckley
Dimensions:	229 x 152 x 24mm (L x W x T)
Format:	Hardcover
Pages:	360
Edition:	UK ed.
ISBN-13:	978-0-12-420246-7
Categories:	Books > Medicine > General issues > Medical equipment & techniques > Medical research Books > Medicine > Other branches of medicine > Pharmacology > General Promotions
LSN:	0-12-420246-2
Barcode:	9780124202467

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