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kmcquade75
05-06-2008, 12:17 AM
Dear Colleagues,

I am in the process of applying for IRB approval for a fine wire EMG
project. I am looking for examples and information how people have
described and written up the risks for informed consent and for human
subjects approval ?

Thanks for any suggestions

Kevin McQuade

Kevin J. McQuade,PT,MPH,PhD
Associate Professor,
Director Motion Analysis Research Lab.
Department of Rehabilitation Medicine
University of Washington
Box 356490
1959 Pacific St.
Seattle,Wa 98195
206.598.5411