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IRB #: 20142639 Approved: 6/15/2015 Do Not Use After: 5/30/2016 UNIVERSITY OF CINCINNATI Medical CONSENT TO PARTICIPATE IN A RESEARCH STUDY Title: Prospective outcomes of management of third molar
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How to fill out an IRB consent form:

01
Begin by carefully reading the instructions provided on the IRB consent form. Familiarize yourself with the purpose and requirements of the form.
02
Provide your personal information accurately. This includes your full name, contact details, and any other requested information.
03
Ensure that all required fields are filled out completely. This may include sections for demographics, medical history, and any other pertinent information.
04
Pay close attention to any sections that require your signature or consent. Read through the accompanying text and make sure you understand the implications of your consent.
05
Include any necessary attachments or supplementary documents as instructed in the form. This may include additional consent forms, participant information sheets, or other supporting materials.
06
Review your completed form for any errors or missing information. Double-check that all sections are filled out correctly and that your responses are accurate.
07
Sign and date the form, as required. Follow any additional instructions provided for submission, such as whether the form needs to be physically signed or if an electronic signature is acceptable.

Who needs an IRB consent form:

01
Researchers conducting studies involving human participants are typically required to obtain IRB (Institutional Review Board) approval and have participants sign a consent form.
02
Participants in research studies involving human subjects are usually required to sign an IRB consent form. This ensures that they understand the purpose, risks, and benefits of the study and agree to participate voluntarily.
03
IRB consent forms are essential in maintaining ethical standards and protecting the rights and welfare of research participants. They are crucial in studies involving sensitive information, interventions, or potential risks to participants.
Note: It's important to consult with your specific institution or research ethics committee for any guidelines or additional requirements regarding filling out an IRB consent form.
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IRB consent form is a document that outlines the purpose, risks, and benefits of a research study and must be signed by participants before they can take part in the study.
Researchers conducting studies involving human subjects are required to file IRB consent forms.
IRB consent forms should be filled out by providing accurate information about the study, risks, benefits, and obtaining signatures from participants.
The purpose of IRB consent forms is to ensure that participants are fully informed about the study they are participating in and voluntarily agree to take part.
IRB consent forms must include study details, risks, benefits, participant rights, confidentiality agreements, and signatures from participants and researchers.
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