Author: Bert Spilker
Edition: 1
Binding: Hardcover
ISBN: 0781774241
Edition: 1
Binding: Hardcover
ISBN: 0781774241
Guide to Drug Development: A Comprehensive Review & Assessment
Written by one of the foremost authorities on clinical trials, drug development, and regulatory affairs, Guide to Drug Development is a comprehensive review of the principles and activities involved in developing new drugs, devices, and other medical products. The book covers many topics not discussed in any other textbook and includes timely discussions on electronic clinical trials, registries of clinical trials, data mining, computer simulations and modeling, and changing regulatory standards. Each chapter includes practical tips, lessons, guides, firsthand stories, quotes from experts, and three to six questions for group discussion. The last three chapters present twelve case studies each on clinical trials, regulatory affairs, and m Categories: Drug Design, Drug development, Pharmaceutical preparations. Contributors: Bert Spilker - Author. Format: Hardcover Read medical textbooks online like Guide to Drug Development here
Anticancer Drug Development Guide (Cancer Drug Discovery and Development)
Anticancer Drug Development Guide (Cancer Drug Discovery and Development) - Beverly Teicher, Paul Andrews
Categories: Drug Design, Drug development, Pharmaceutical preparations. Contributors: Bert Spilker - Author. Format: Hardcover
author bert spilker format hardback language english publication year 01 09 2008 subject medicine subject 2 medical nursing ancillary services title guide to drug development a comprehensive review and assessment author spiker bent ph dmd publisher lippincott williams wilkins publication date sep 01 2008 pages 1277 binding hardcover edition 1 st dimensions 8 75 wx 11 25 hx 2 00 d isbn 0781774241 subject medical pharmacology description written by one of the foremost authorities on clinical t
Guide to Drug Development: A Comprehensive Review and Assessment, ISBN-13: 9780781774246, ISBN-10: 0781774241
Guide to Drug Development Online
The book covers many topics not discussed in any other textbook and includes timely discussions on electronic clinical trials, registries of clinical trials, data mining, computer simulations and modeling, and changing regulatory standards
The last three chapters present twelve case studies each on clinical trials, regulatory affairs, and m
