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Safety pharmacology in pharmaceutical developmentapproval and post marketing surveillance /

Record Type:	Language materials, printed : Monograph/item
Title/Author:	Safety pharmacology in pharmaceutical development/ Shayne C. Gad.
Reminder of title:	approval and post marketing surveillance /
Author:	Gad, Shayne C.,
other author:	Gad, Shayne C.,
Published:	Boca Raton, FL :CRC Press, : c2012.,
[NT 15000922]:	2nd ed.
Description:	1 online resource (xv, 197 p.) :ill. :
Notes:	Rev. ed. of: Safety pharmacology in pharmaceutical development and approval. c2004.
基督教聖經之智慧書導讀 :	"This book covers the regulatory required evaluation and study of the potentially adverse pharmacological effects of new drugs, from the general regulatory requirements to the specific studies that must be done and how they are performed and interpreted. Based on more than 30 years of direct experience, the author describes tricks and practical insights for making studies work and understanding why they don't. The second edition includes current regulations (US FDA and international especially Europe and Japan) and updated test methods, interpretation, and science"--Provided by publisher.
Subject:	Drugs - Toxicology. -
Online resource:	http://www.crcnetbase.com/isbn/9781439845684
ISBN:	9781439845684 (electronic bk.)

Safety pharmacology in pharmaceutical developmentapproval and post marketing surveillance /
Gad, Shayne C.,1948-

Safety pharmacology in pharmaceutical developmentapproval and post marketing surveillance /[electronic resource] :Shayne C. Gad. - 2nd ed. - Boca Raton, FL :CRC Press,c2012. - 1 online resource (xv, 197 p.) :ill.

Rev. ed. of: Safety pharmacology in pharmaceutical development and approval. c2004.

Includes bibliographical references and index.

Safety pharmacology: background, history, issues and concerns -- Regulatory requirements: ICH, FDA, EMA, and Japan -- Principles of screening and study design -- Cardiovascular system -- Central nervous system -- Respiratory system -- Renal function -- Gastrointestinal system -- Immune system.

"This book covers the regulatory required evaluation and study of the potentially adverse pharmacological effects of new drugs, from the general regulatory requirements to the specific studies that must be done and how they are performed and interpreted. Based on more than 30 years of direct experience, the author describes tricks and practical insights for making studies work and understanding why they don't. The second edition includes current regulations (US FDA and international especially Europe and Japan) and updated test methods, interpretation, and science"--Provided by publisher.

ISBN: 9781439845684 (electronic bk.)

LCCN: 2012009446Subjects--Topical Terms:

220299
Drugs
--Toxicology.

LC Class. No.: RA1238 / .G333 2012

Dewey Class. No.: 615.7/04

National Library of Medicine Call No.: 2012 F-386

Safety pharmacology in pharmaceutical developmentapproval and post marketing surveillance /
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245 1 0 $a Safety pharmacology in pharmaceutical development $h [electronic resource] : $b approval and post marketing surveillance / $c Shayne C. Gad.
250 $a 2nd ed.
260 $a Boca Raton, FL : $b CRC Press, $c c2012.
300 $a 1 online resource (xv, 197 p.) : $b ill.
500 $a Rev. ed. of: Safety pharmacology in pharmaceutical development and approval. c2004.
504 $a Includes bibliographical references and index.
505 0 $a Safety pharmacology: background, history, issues and concerns -- Regulatory requirements: ICH, FDA, EMA, and Japan -- Principles of screening and study design -- Cardiovascular system -- Central nervous system -- Respiratory system -- Renal function -- Gastrointestinal system -- Immune system.
520 $a "This book covers the regulatory required evaluation and study of the potentially adverse pharmacological effects of new drugs, from the general regulatory requirements to the specific studies that must be done and how they are performed and interpreted. Based on more than 30 years of direct experience, the author describes tricks and practical insights for making studies work and understanding why they don't. The second edition includes current regulations (US FDA and international especially Europe and Japan) and updated test methods, interpretation, and science"--Provided by publisher.
588 $a Description based on print version record.
650 0 $2 96060 $a Drugs $x Toxicology. $3 220299
650 0 $a Drugs $x Safety measures. $3 351601
650 0 $a Drug development $x Safety measures. $3 405217
650 1 2 $2 96060 $a Drug Evaluation, Preclinical. $3 253578
650 2 2 $2 96060 $a Drug Approval. $3 214022
650 2 2 $2 96060 $a Product Surveillance, Postmarketing. $3 254389
650 2 2 $a Toxicity Tests. $3 299491
700 1 $2 97000 $a Gad, Shayne C., $d 1948- $3 255793
856 4 0 $u http://www.crcnetbase.com/isbn/9781439845684