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Memorial Sloan Kettering Cancer Center IRB Protocol IRB#: 09069 INFORMED CONSENT FOR CLINICAL RESEARCH Refinement of the PatientReported Outcomes Version of the Common Terminology Criteria for Adverse
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How to fill out irb 09-069 informed consent
How to fill out IRB 09-069 informed consent:
01
Read the entire document carefully to understand its purpose and requirements.
02
Fill in the participant's name, contact information, and any other identifying details requested.
03
Provide a clear and concise description of the study or research project.
04
Explain the objectives, potential risks, benefits, and any incentives associated with participating in the study.
05
Ensure that the participant understands their right to decline participation or withdraw at any time without consequences.
06
Clearly outline the procedures or interventions involved in the study and any necessary instructions or precautions.
07
Provide contact information for the research team or principal investigator in case the participant has any questions or concerns.
08
Include any additional information or disclosures required by the specific research institution or governing body.
09
Ensure that the participant or their legally authorized representative signs and dates the consent form.
10
Make a copy of the completed, signed consent form for both the participant and the research team's records.
Who needs IRB 09-069 informed consent:
01
Researchers conducting studies or research projects that involve human participants.
02
Participants who are being asked to provide consent and agree to participate in the study.
03
Institutional Review Boards (IRBs) or ethics committees responsible for reviewing and approving research protocols for compliance with ethical guidelines.
Note: It is important to consult the specific requirements set forth by the IRB or the research institution to ensure compliance with their guidelines.
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