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INFORMATION AND CONSENT FORM RESEARCH ACTIVITY Title: Development of Endometriosis Test Kit Lateral Flow Device Research team Julien Le Roy, PhD, Principal Investigator, Collge La Cit, jleroy@lacitec.on.ca,
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What is information and consent form?
An information and consent form is a document used to explain the details of a study, treatment, or procedure to participants and obtain their permission to proceed.
Who is required to file information and consent form?
Researchers, clinicians, and organizations conducting studies involving human subjects are required to file an information and consent form.
How to fill out information and consent form?
To fill out an information and consent form, provide clear and comprehensive information about the study, risks, benefits, confidentiality, and obtain the participant's signature to indicate their consent.
What is the purpose of information and consent form?
The purpose of the information and consent form is to ensure that participants are fully informed about the study or treatment, understand their rights, and voluntarily agree to participate.
What information must be reported on information and consent form?
The information must include the purpose of the study, procedures involved, potential risks and benefits, confidentiality assurances, and contact information for questions or concerns.
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