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APPROVED BY THE YALE UNIVERSITY IRB 5/4/2022 Yale Opioid Stewardship Pilot Randomized Clinical Trial Page 1 of 12CLINICAL RESEARCH INFORMED CONSENT FORM AND AUTHORIZATION TO USE AND DISCLOSE PROTECTED

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How to fill out irb submission form

01

Obtain the IRB submission form from the appropriate institution or organization.

02

Fill out all required sections of the form, including study title, principal investigator information, study procedures, risks and benefits, and consent process.

03

Attach any supporting documents or materials, such as study protocols, recruitment materials, and consent forms.

04

Review the completed form for accuracy and completeness before submitting.

05

Submit the form to the IRB for review and approval.

Who needs irb submission form?

01

Researchers conducting human subjects research

02

Students conducting research projects involving human participants

03

Institutions or organizations requiring IRB approval for research studies

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What is irb submission form?

The IRB submission form is a document required for researchers to submit proposals for review by an Institutional Review Board (IRB) to ensure ethical standards in research involving human subjects.

Who is required to file irb submission form?

Researchers and institutions conducting studies involving human subjects are required to file an IRB submission form.

How to fill out irb submission form?

To fill out the IRB submission form, one must provide detailed information about the study, including objectives, methodology, participant recruitment, informed consent processes, and potential risks to participants.

What is the purpose of irb submission form?

The purpose of the IRB submission form is to ensure that research studies protect the rights and welfare of human subjects by undergoing ethical review.

What information must be reported on irb submission form?

The IRB submission form must report information including the study's title, principal investigator's details, study design, participant demographics, informed consent procedures, and anticipated risks and benefits.

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