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Informed ConsentExcept where specifically waived or altered by the IRB under Section I.K.34 of the University of Maine\'s Policies and Procedures for the Protection of Human Subjects of Research,
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How to fill out informed consent checklist

01
Start by reviewing the informed consent checklist form provided.
02
Familiarize yourself with the purpose and importance of the informed consent process.
03
Make sure you have all the necessary information about the research study or medical procedure.
04
Carefully read each item on the checklist and understand its meaning.
05
Tick or mark the checkbox next to each item that you have completed or agree to.
06
If there are any items that you do not understand or have concerns about, seek clarification from the authorized personnel.
07
Once you have reviewed and completed the checklist, sign and date it to indicate your agreement and understanding.
08
Keep a copy of the completed checklist for your records.

Who needs informed consent checklist?

01
Anyone participating in a research study or undergoing a medical procedure that involves potential risks or requires informed consent.

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An informed consent checklist is a tool used to ensure that all necessary information has been communicated and understood by participants before they agree to participate in a study or procedure.
Researchers, healthcare providers, and organizations conducting studies or trials that involve human participants are typically required to file an informed consent checklist.
To fill out an informed consent checklist, one must carefully review all required components, ensure all relevant information is provided, and obtain signatures from participants indicating their understanding and agreement.
The purpose of an informed consent checklist is to protect participants by ensuring they are fully informed about the nature, risks, benefits, and procedures of the study, thereby promoting ethical research practices.
The informed consent checklist must include information about the study's purpose, procedures, risks, benefits, confidentiality, and the participant's right to withdraw at any time.
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