CRA's Guide to Monitoring Clinical Research

Weeks-Rowe, Elizabeth

Book Information
Edition:	4th
Publisher:	CenterWatch, Inc.
ISBN:	1-930624-73-5 (1930624735)
ISBN-13:	978-1-930624-73-3 (9781930624733)
New Edition:	1-60430-088-4
Old Edition:	1-930624-60-3
Binding:	Softcover
Copyright:	2016
Publish Date:	06/16
Weight:	2.66 Lbs.
Pages:	732
Subject Class:	PHM (Pharmacy and Pharmaceutical Industry)
Remarks:	A New Edition of this Title is Available
Return Policy:	Non-Returnable.
Contributing Authors:	View

Class Specifications
Discipline:	Pharmacology
Subject Definition:	Clinical Trials as Topic-Standards; Drug Approval-Org & Adm
NLM Class:	QV 771
LC Class:	RM301.27
Abstract:	The CRA's Guide to Monitoring Clinical Research, fourth edition, continues to be a vital resource for both novice and experienced CRAs seeking to learn more about the field of monitoring or to better understand their roles and responsibilities as the industry becomes more global and technologically focused. This edition includes helpful tips and strategies, checklists, personal experiences, traveling tips, key takeaways and exercises. With new and updated chapters on the evolving CRA roles and responsibilities, monitoring for device and biologic trials, risk-based monitoring, globalization of studies, EMR, web-driven data collection, the sub-PI role, and more, The CRA's Guide is a must-have training and educational tool that you'll refer to time and time again.

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