revised_consent_form - INSTRUCTIONS FOR INVESTIGATOR The...

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INSTRUCTIONS FOR INVESTIGATOR The following is a template for a complete informed consent document. As a guide, it can be partially revised to fit your study. However, the first two (2) paragraphs and all questions need to be included, as required the by the Office of Human Research Protections. If you choose to alter or waive consent for your study, you must provide justification to do so. Fill out the appropriate portion of the Request for Waiver or Alteration of Consent and attach it to your IRB application. The form can be accessed at If a question is not applicable to your study, simply insert n/a. You should also eliminate suggested language (in brackets and red type) if not pertinent to your study, to enhance participant comprehension. If used for a parent/legal guardian, alter language to refer to child. Should you have any questions or need additional information, please do not hesitate to contact my office. Compliance Officer Box 134 Sam Ingram Building 011B (615) 494-8918
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Middle Tennessee State University Institutional Review Board Informed Consent Document for Research Please remove all instruction areas in red and any non applicable italicized information. Principal Investigator:
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This note was uploaded on 09/27/2011 for the course FINACE 6710 taught by Professor Homaifar during the Spring '11 term at Middle Tennessee State University.

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revised_consent_form - INSTRUCTIONS FOR INVESTIGATOR The...

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