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CONSENT FORM - Adults INSTRUCTIONS - Texas Tech University - depts ttu

CONSENT FORM - Adults INSTRUCTIONS - Texas Tech University - depts ttu 2025

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The document outlines the purpose and requirements of a consent form for research involving human subjects. It emphasizes the importance of clear communication, ensuring that consent forms are understandable, written at an appropriate reading level, and include all necessary information about the study. The consent process is highlighted as crucial for participant understanding and researcher assurance. Additionally, it specifies that consent forms should avoid legal jargon, be written in the second person, and must be retained by investigators for three years after IRB approval.

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Do informed consent forms expire?

Answer: No. Neither the Common Rule (38 CFR Part 16) nor VHA Handbook 1200.05 requires that expiration dates appear on informed consent forms. Each IRB has the authority to determine whether or not expiration dates are to appear on the consent forms that it approves.

Do consent forms expire?

DHHS regulations (45 CFR 46.115) require that an IRB keep approved sample consent forms for at least three years after the completion of the research.

How long is a signed informed consent valid?

ANSWER. CMS does not provide a specific timeframe for how long consumer consent documentation can be effective. You may determine the duration of consent with your consumers (or their authorized representative).

How long does an informed consent form last?

How long is a consent form good for? Generally, there is no strict rule on how long in advance of the procedure informed consent can or should be obtained. Although some procedures have specific requirements (e.g. sterilization). Otherwise, physician discretion and hospital policy govern.

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