№ lp_1_2_37109
Institutional research ethics consent template outlining required language, structure, and content for participant information and voluntary consent in minimal risk clinical studies conducted at a Canadian university.
Institution: University of British Columbia
Document type: Clinical informed consent form template
Study risk level: Minimal risk
Regulatory scope: Not regulated by Health Canada or the U.S. Food and Drug Administration
Jurisdiction: British Columbia, Canada
Intended use: Non-regulated clinical research studies
Target audience: Research participants from the general population
Reading level: Grade 7
Applicable populations: Adults and, where applicable, pediatric participants with parental permission and child assent
Ethics oversight: Research Ethics Board (REB)
Source type: Institutional research ethics documentation
Price: 8 / 10 USD
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