Kentucky Specimen Repository Agreement

State:
Multi-State
Control #:
US-EG-9160
Format:
Word; 
Rich Text
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Description

DNA Specimen Repository Agreement between The University of North Texas Health Science Center at Forth Worth and GeneLink, Inc. dated June 21, 1995. 12 pages
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FAQ

Obtaining Written or Verbal Informed Consent. Obtaining consent involves explaining the research and assessing participant comprehension using a consent document, usually a written consent form or information sheet, as a guide for the verbal explanation of the study. Obtaining and Documenting Informed Consent - UCSF IRB ucsf.edu ? obtaining-and-documenting-inform... ucsf.edu ? obtaining-and-documenting-inform...

Informed consent means that the purpose of the research is explained to them, including what their role would be and how the trial will work. A central part of the informed consent process is the informed consent document. Informed Consent for Clinical Trials - FDA fda.gov ? patients ? informed-consent-clinic... fda.gov ? patients ? informed-consent-clinic...

I have read and understand the information in this form. I have been encouraged to ask questions and all of my questions have been answered to my satisfaction. I have also been informed that I can withdraw from the study at any time. By signing this form, I voluntarily agree to participate in this study. SAMPLE INFORMED CONSENT FOR SOCIAL AND BEHAVIORAL ... missouristate.edu ? Sample_ICF_project_Behav missouristate.edu ? Sample_ICF_project_Behav

Generally not. Most retrospective chart reviews involve a large number of records, and therefore the IRB would consider it impracticable (not possible) to do the study if informed consent and authorization were required. However, the investigator must answer the waiver of consent/authorization questions (section IV.

The informed consent should make clear that all such tissue samples are potential sources of genetic information about individuals. In addition, it should state clearly that names and other personal identifiers of subjects will not be sent to any recipients of the blood or tissue samples.

Informed consent must be obtained from patients for the use of organs or tissues in clinical research. Ethical and legal considerations regarding the ownership ... - NCBI nih.gov ? articles ? PMC3440234 nih.gov ? articles ? PMC3440234

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Kentucky Specimen Repository Agreement