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Informed consent :a guide to the ris...

Getz, Kenneth

Informed consent :a guide to the risks and benefits of volunteering for clinical trials /

Record Type:	Language materials, printed : Monograph/item
Title/Author:	Informed consent :/ Kenneth Getz & DeborahBorfitz ; with a foreword by Paul Gelsinger
Reminder of title:	a guide to the risks and benefits of volunteering for clinical trials /
remainder title:	Risks and benefits of volunteering for clinical trials
Author:	Getz, Kenneth
other author:	Borfitz, Deborah
Published:	Boston, MA :CenterWatch, : c2002,
Description:	306 p. :ill. ; : 21 cm;
Subject:	Informed consent (Medical law) - United States -
ISBN:	1930624093 (pbk.):

Informed consent :a guide to the risks and benefits of volunteering for clinical trials /
Getz, Kenneth

Informed consent :a guide to the risks and benefits of volunteering for clinical trials /Risks and benefits of volunteering for clinical trialsKenneth Getz & DeborahBorfitz ; with a foreword by Paul Gelsinger - Boston, MA :CenterWatch,c2002 - 306 p. :ill. ;21 cm

Clinical trials-a very human enterprise --Ch. 1

ISBN: 1930624093 (pbk.):NT911Subjects--Topical Terms:

223957
Informed consent (Medical law)
--United States

National Library of Medicine Call No.: W 20.55 / .H9 G394i 2002

Informed consent :a guide to the risks and benefits of volunteering for clinical trials /
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100 1 $2 97000 $a Getz, Kenneth $3 223955
245 1 0 $a Informed consent : $b a guide to the risks and benefits of volunteering for clinical trials / $c Kenneth Getz & DeborahBorfitz ; with a foreword by Paul Gelsinger
246 3 0 $a Risks and benefits of volunteering for clinical trials
260 # $a Boston, MA : $c c2002 $b CenterWatch,
300 $a 306 p. : $b ill. ; $c 21 cm
505 0 0 $g Ch. 1 $t Clinical trials-a very human enterprise -- $g Ch. 2 $t Why people participate -- $g Ch. 3 $t Doing your homework -- $g Ch. 4 $t Giving your informed consent -- $g Ch. 5 $t Historical events that have shaped human subject protections -- $g Ch. 6 $t Vulnerable populations -- $g Ch. 7 $t What to do when things go wrong -- $g Ch. 8 $t Finding clinical trials -- $t Afterward -- $g App. A $t Glossary of terms -- $g App. B $t A history of regulations affecting patient protection in clinical research $g App. C $t World Medical Association Declaration of Helsinki -- $g App. D $t The Belmont Report $g App. E $t 45 CFR 46 Federal Policy forthe Protection of Human Subjects -- $g App. G $t 21 CFR 50 Protection of Human Subjects -- $g App. H $t Form 1572 -- $g App. I $t Directory of health associations -- $g Directory of biotechnology and pharmaceutical companies -- About theauthors
650 # 0 $2 96060 $a Informed consent (Medical law) $z United States $3 223957
650 2 2 $2 96060 $a PATIENT ACCEPTANCE OF HEALTH CARE. $3 197836
650 1 2 $2 96060 $a INFORMED CONSENT. $3 199182
650 # 0 $2 96060 $a Clinical trials. $3 213847
650 # 0 $2 96060 $a Human experimentation in medicine $3 223956
700 1 # $2 97000 $a Borfitz, Deborah $3 223954
900 $c 到館:2003/07/16 $d 編目:2003/07/16