A guide to informed consent for clinician-investigators.

Abstract:

:Informed consent in clinical research is a matter of both ethics and federal regulation. A research subject must enter a study voluntarily, be informed about risks and benefits, and understand the difference between experiment and treatment.

journal_name

Cleve Clin J Med

authors

Bramstedt KA

doi

10.3949/ccjm.71.11.907

subject

Has Abstract

pub_date

2004-11-01 00:00:00

pages

907-10

issue

11

eissn

0891-1150

issn

1939-2869

journal_volume

71

pub_type

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