|
![]() |
|||
|
||||
OverviewThe National Institutes of Health and the National Science Foundation together fund more than $40 billon of research annually in the United States and around the globe. These large public expenditures come with strings, including a complex set of laws and guidelines that regulate how scientists may use NIH and NSF funds, how federally funded research may be conducted, and who may have access to or own the product of the research. Until now, researchers have had little instruction on the nature of these laws and how they work. But now, with Robert P. Charrow’s Law in the Laboratory, they have a readable and entertaining introduction to the major ethical and legal considerations pertaining to research under the aegis of federal science funding. For any academic whose position is grant funded, or for any faculty involved in securing grants, this book will be an essential reference manual. And for those who want to learn how federal legislation and regulations affect laboratory research, Charrow’s primer will shed light on the often obscured intersection of government and science. Full Product DetailsAuthor: Robert P. CharrowPublisher: The University of Chicago Press Imprint: University of Chicago Press Dimensions: Width: 1.60cm , Height: 0.20cm , Length: 2.30cm Weight: 0.567kg ISBN: 9780226101644ISBN 10: 0226101649 Pages: 336 Publication Date: 15 July 2010 Audience: College/higher education , Postgraduate, Research & Scholarly Format: Hardback Publisher's Status: Active Availability: Out of stock ![]() The supplier is temporarily out of stock of this item. It will be ordered for you on backorder and shipped when it becomes available. Table of ContentsReviewsA superb review of the complex laws, regulations, and generally accepted procedure that relate to the conduct of biomedical research in the United States. Law in the Laboratory should be required reading for deans or heads of research, for academic faculty, for federal regulators, and for graduate students as a part of their introduction to legal and ethical aspects of biomedical research. - Katherine High, University of Pennsylvania Author InformationRobert P. Charrow is a lawyer who has served on a presidential election committee, as principal deputy general counsel in the U.S. Department of Health and Human Services, as vice chair of the Clinical Research Interest Group of the Health Law Section of the American Bar Association, and as a member of the Board of Advisors for the Institute of Virology at the University of Maryland. Tab Content 6Author Website:Countries AvailableAll regions |