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Protocol 20200481 March 25, 2022 Page 1 of 13Informed ConsentINFORMED CONSENT/AUTHORIZATION FOR PARTICIPATION IN RESEARCH A Phase Ib Trial of Preoperative ShortCourse Chemoradiotherapy followed by
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Begin with the title of the document, 'Informed Consent/Authorization'.
02
Provide a brief description of the procedure or research study.
03
Include a section detailing the purpose of the consent and what it entails.
04
Clearly outline potential risks and benefits associated with the procedure.
05
List any alternatives to the proposed procedure or study.
06
Include a privacy statement explaining how the individual's information will be protected.
07
Provide space for the participant to ask questions and have them answered before they sign.
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Include a signature line for the participant and date of signing.
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Add a section for the witness signature, if required.

Who needs informed consentauthorization for?

01
Individuals participating in clinical trials.
02
Patients undergoing medical procedures.
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Participants in psychological studies.
04
Volunteers in research studies involving their personal data.
05
Parents/guardians providing consent for minors participating in studies.
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Informed consent authorization is a process that ensures individuals are fully aware of the risks and benefits associated with a procedure or participation in a study before agreeing to it.
Researchers, healthcare providers, and institutions conducting studies or medical procedures that involve human subjects are required to file informed consent authorization.
To fill out an informed consent authorization, provide details about the study or procedure, information on risks and benefits, and obtain the signature of the participant, ensuring they understand what they are agreeing to.
The purpose of informed consent authorization is to protect the rights and welfare of participants by ensuring they are informed and voluntarily agree to partake in a study or procedure.
Informed consent authorization must report details about the study, potential risks, benefits, confidentiality measures, and the right to withdraw consent at any time.
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