Drug-Drug Interactions: Scientific and Regulatory Perspectives

Drug-Drug Interactions: Scientific and Regulatory Perspectives on ScienceDirect(Opens new window)
Hardbound, 304 Pages
Published: OCT-1997
ISBN 10: 0-12-032944-1
ISBN 13: 978-0-12-032944-1
Imprint: ACADEMIC PRESS


Edited by
Albert Li, In Vitro Technologies, Inc., and University of Maryland Technology Center, Baltimore, Maryland, U.S.A.

Series Editor:
J. August, John Hopkins University; Department of Pharmacology, Baltimore, Maryland, U.S.A.
Ferid Murad, University of Texas Medical School, Houston, U.S.A.
M. Anders, University of Rochester; Department of Pharmacology, New York, U.S.A.
Joseph Coyle, McLean Hospital, Harvard Medical School, Belmont, Massachusetts, U.S.A.

Description
Drug–Drug Interactions is a comprehensive review of the scientific and regulatory perspectives of drug–drug interactions from the point-of-view of academia, industry, and government regulatory agencies. This book is intended for professionals in the pharmaceutical industry, health care, and governmental regulatory agencies. Topics of interest include the mechanistic understanding of drug–drug interactions, the prediction of drug–drug interaction potential of new drugs, and the avoidance of clinically significant drug–drug interaction in patients.

Included in series
Advances in Pharmacology

Audience:
Professionals in the pharmaceutical industry, health care industry, and governmental regulatory agencies. Students and researchers in the areas of pharmacology, toxicology, pharmacokinetics, and medicine.


 
Last update: 5 Nov 2011