A guide to informed consent for clinician-investigators

Katrina A. Bramstedt

doi:10.3949/ccjm.71.11.907

A guide to informed consent for clinician-investigators

Katrina A. Bramstedt^*

^*Corresponding author for this work

Research output: Contribution to journal › Review article › Research › peer-review

6 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 language	English
Pages (from-to)	907-910
Number of pages	4
Journal	Cleveland Clinic Journal of Medicine
Volume	71
Issue number	11
DOIs	https://doi.org/10.3949/ccjm.71.11.907
Publication status	Published - Nov 2004
Externally published	Yes

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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.",

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A guide to informed consent for clinician-investigators

Abstract

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