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Manual of Drug Safety And Pharmacovigilance
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Binding: Paperback
Dewey Decimal Number: 615.7042
EAN: 9780763738891
Edition: 1st
ISBN: 0763738891
Label: Jones & Bartlett Publishers
Manufacturer: Jones & Bartlett Publishers
Number Of Items: 1
Number Of Pages: 292
Publication Date: December 01, 2006
Publisher: Jones & Bartlett Publishers
Release Date: December 01, 2006
Studio: Jones & Bartlett Publishers
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Editorial Review:
Drug Safety 101! A how-to manual for newcomers to the field of drug safety, clinical research, regulatory affairs, law and other domains touching on pharmacology who wish to learn the theory and the practicalities of drug safety (pharmacovigilance) and side effects, this comprehensive and practical guide provides essential information on drug safety and regulations, including recognizing, monitoring, reporting, and cataloging serious adverse drug reactions. Whether you're working in drug safety, clinical research, regulatory affairs, epidemiology, marketing and sales, nursing, pharmacoepidemiology, or another area in the pharmaceutical industry, FDA (or other regulatory agency), academia, hospital (especially pharmacy or formulary committee) are a lawyer, writer, or other professional who needs to know the details of drug safety and side effects, training nurses, pharmacists and PharmD and PhD pharmacology students or medical students, this is the book for you! This book teaches the ins and outs of drug safety in the industry, a hospital, FDA, and other health agencies both in the US and around the world, and presents critical information about what is done in the industry and FDA when confronted with a drug safety problem. Book includes a free CD-ROM!
Customer Reviews
Average Rating: 
Rating: - Long Overdue
Working in Drug Safety for the past five years, I have waited for a book specific to the field. Previous understanding and knowledge was reduced to searching the CFR, reading ICH regulations, memorizing company SOP's, attending training presentations, etc. The book brings all the scattered pieces of information and regulations into a cohesive organization that allows it to be used as a comprehensive read or as a reference for drug safety information.
If read from chapter to chapter, ... Read More
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