A guide to informed consent for clinician-investigators

Katrina A. Bramstedt*

*Corresponding author for this work

Research output: Contribution to journalReview articleResearchpeer-review

4 Citations (Scopus)

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.

Original languageEnglish
Pages (from-to)907-910
Number of pages4
JournalCleveland Clinic Journal of Medicine
Volume71
Issue number11
DOIs
Publication statusPublished - Nov 2004
Externally publishedYes

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