| informed consent |
a legal document that explains a course of treatment, the risks, benefits, and possible alternatives; the process by which patients agree to treatment.
출처: www.rch.org.au/ceed/disorders.cfm
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| informed consent |
Before patients make the decision to participate in a clinical trial, they are given detailed information about the study, including what treatments will be tested, the possible side effects and the time commitment required.
출처: www.seattlecca.org/patientsandfamilies/WhatAreClin...
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| informed consent |
Person's agreement to allow something to happen, such as a medical procedure, that is based on full disclosure of the facts necessary to make an intelligent decision.
출처: www.edgarsnyder.com/resources/terms/i.html
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| informed consent |
the ongoing dialogue between researchers and participants that addresses patient concerns and questions and ensures patient protection throughout the trial
출처: www.gene.com/gene/pipeline/trial-education/glossar...
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| informed consent |
A person's voluntary agreement, based upon adequate knowledge and understanding of relevant information, to participate in research or to undergo a diagnostic, therapeutic, or preventive measure. In giving informed consent, subjects may not waive or appear to waive any of their legal rights, or release or appear to release the investigator, the sponsor, the institution or agents thereof from liability for negligence.
출처: www.virginia.edu/vprgs/irbsbsterminology.html
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