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Consent Forms

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Definition: Documents describing a medical treatment or research project, including proposed procedures, risks, and alternatives, that are to be signed by an individual, or the individual's proxy, to indicate his/her understanding of the document and a willingness to undergo the treatment or to participate in the research.      Other names Documents, Informed Consent; Document, Informed Consent; Consent Form; Consent Documents, Informed; Consent Document, Informed; Consent Document; Informed Consent Documents; Informed Consent Form; Informed Consent Document; Informed Consent Forms; Consent Documents

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Sources: NLM Medical Subject Headings, NIH UMLS, Drugs@FDA, FDA AERS original data copyright United States Government. No endorsement implied. Last modified 6/6/2012

Warning: the drugs or drug combinations referred to here may be similar or related, but are not be the same ones and may not have the same pharmacological action as other substances described on the same page or in the same row. Please refer to product monograph or to your doctor
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