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GARRICK INSTITUTE INSTITUTIONAL REVIEW BOARD STANDARDIZED INFORMED CONSENT Reinformed Consent FormParticipation in a biomedical/physiological research project/investigationTitle of the research project/investigation:(S1)Statement from the participant:I have been given written and verbal information about the research project to a satisfactory degree and I know enough about the
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How to fill out ci-irb standardized informed consent

01
Step 1: Read through the ci-irb standardized informed consent document carefully to understand its purpose and the information it requires.
02
Step 2: Begin by providing basic information about the participant, including their name, age, gender, and contact details.
03
Step 3: Clearly explain the purpose of the study and the procedures that will be conducted as part of the research.
04
Step 4: Describe any potential risks or discomforts that the participant may experience during the study and provide information on how these will be managed.
05
Step 5: Outline the potential benefits that the participant may receive from participating in the study.
06
Step 6: Discuss the confidentiality and privacy measures that will be taken to protect the participant's personal information.
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Step 7: Clearly state that participation in the study is voluntary and that the participant has the right to withdraw at any time without penalty.
08
Step 8: Provide contact information for the researcher or study coordinator in case the participant has any questions or concerns.
09
Step 9: Establish a section for the participant to sign and date to indicate their informed consent.
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Step 10: Make copies of the completed ci-irb standardized informed consent document, with one copy provided to the participant for their records.

Who needs ci-irb standardized informed consent?

01
The ci-irb standardized informed consent is required for individuals who are participating in research studies that are overseen by the ci-irb (Clinical Investigator-Initiated Investigational Review Board). This includes both adult and minor participants.
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Standardized informed consent provided by a Clinical Investigator Institutional Review Board.
Clinical investigators conducting research involving human subjects.
By following the guidelines and templates provided by the institution's IRB.
To ensure that subjects are fully informed about the research study before participating.
Study procedures, risks and benefits, confidentiality, and subject rights.
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2020 ci carrick irb s1 anonymized s2 contra institutional participant physiological standardized publications consultation bio

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