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PARTICIPANT INFORMATION and CONSENT FERTILE OF RESEARCH PROJECT: David Mowafaghian Center for Brain Health BiobankPrincipal Investigator:Dr. Lynn A. Raymond, MD, PhD Director, David Mowafaghian Center

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How to fill out participant information and consent

01

Start by providing clear instructions on how participants can access the information and consent form.

02

Include all the necessary fields for participants to fill out, such as their personal details, contact information, and signature.

03

Clearly explain the purpose of collecting this information and how it will be used in the research study.

04

Provide options for participants to indicate their consent, such as checkboxes or signature lines.

05

Make sure to include a section for participants to ask any questions or provide additional comments before signing.

Who needs participant information and consent?

01

Researchers conducting a study that involves human subjects

02

Institutional Review Boards (IRBs) or ethics committees overseeing the research study

03

Funding agencies or sponsors of the research study

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What is participant information and consent?

Participant information and consent refers to the details about individuals participating in a study or research project, including their personal information and their agreement to participate.

Who is required to file participant information and consent?

Researchers, institutions, or organizations conducting a study or research project are required to file participant information and consent.

How to fill out participant information and consent?

Participant information and consent forms can be filled out by providing accurate personal details of the participants and obtaining their consent to participate in the study.

What is the purpose of participant information and consent?

The purpose of participant information and consent is to ensure that individuals participating in a study or research project are fully informed about the research, their involvement, and their rights.

What information must be reported on participant information and consent?

Participant information and consent forms typically include details such as participant demographics, contact information, study procedures, risks, benefits, and confidentiality agreements.

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