| informed consent |
An individual willingly agrees to participate in an activity after first being advised of the risks and benefits. Source : Human Genome Project Information
출처: www.genomecanada.ca/GCglossaire/glossaire/index.as...
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| informed consent |
legally required procedure to ensure that a patient knows about the potential risks and benefits of a treatment before it is started.
출처: www.lymphomainfo.net/lymphoma/glossary.html
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| informed consent |
The process of learning key facts about a clinical trial before participating, including:
출처: www.mdsupport.org/glossary.html
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| informed consent |
An agreement to participate in a trial that's given after a potential participant has reviewed all available information about the treatment. Participants in a clinical trial must be fully informed of the potential risks and benefits of the experimental treatment as well as other treatment options. There must be no penalties for declining to participate or for withdrawing from the trial at any time.
출처: www.mayoclinic.com/invoke.cfm
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| information system |
An organized collection, storage, and presentation system of data and other knowledge for decision making, progress reporting, and for planning and evaluation of programs. It can be either manual or computerized, or a combination of both.
출처: www.ojp.usdoj.gov/BJA/evaluation/glossary/glossary...
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