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CONSENT/PERMISSION/ASSENT FORM FOR A DATA &/OR SPECIMEN REPOSITORY (TEMPLATE VERSION: 10/28/15) This form may be used for collection of data and/or any specimens of body materials (e.g., surgically
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How to fill out irb consent and assent

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How to fill out irb consent and assent

01
Review the IRB guidelines and the specific consent and assent form provided by the institution.
02
Fill in all required information about the study, including the purpose, procedures, risks, benefits, and contact information.
03
Ensure that the language used is clear and understandable to the participants.
04
Provide space for participants to sign and date the form, as well as a place for the researcher to sign as well.
05
Make copies of the completed form for both the participant and the researcher to keep.

Who needs irb consent and assent?

01
Anyone conducting research involving human subjects that is funded or overseen by an institution with an Institutional Review Board (IRB) needs to obtain IRB consent and assent.

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IRB consent refers to the informed consent obtained from participants involved in research studies, ensuring they understand the study's purpose, procedures, risks, and benefits. Assent is the agreement from minors or individuals who cannot fully consent, affirming that they understand the study in an age-appropriate manner.
Researchers and institutions conducting human subjects research are required to file IRB consent and assent forms to ensure ethical standards are met and participants are fully informed and agree to participate.
IRB consent and assent forms should be filled out by providing clear, understandable information about the study, including its purpose, procedures, potential risks, benefits, and the voluntary nature of participation. It's important to ensure the language is appropriate for the target audience.
The purpose of IRB consent and assent is to protect the rights and welfare of research participants by ensuring they are informed about the nature of the research and that they voluntarily agree to participate.
Information reported on IRB consent and assent includes the study title, purpose, procedures, potential risks and benefits, confidentiality assurances, contact information for questions, and the voluntary nature of participation.
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