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Department of Public Health Institutional Review Board 313 N. Figueroa St., Room 127 Los Angeles, CA 90012 Phone: (213) 2888675 Email: irb@ph.lacounty.gov http://publichealth.lacounty.gov/irb/Consent
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How to fill out request for exempt review

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How to fill out request for exempt review

01
Start by gathering all the necessary information and documents required for the exempt review.
02
Identify the specific criteria for which you are seeking exemption.
03
Write a concise and clear statement explaining why your request qualifies for exempt review.
04
Include any relevant supporting documents or evidence to strengthen your case.
05
Fill out the request form, ensuring that all fields are completed accurately and thoroughly.
06
Double-check your request for any errors or omissions before submitting it.
07
Submit the completed request for exempt review to the designated authority or department.

Who needs request for exempt review?

01
Individuals or organizations that believe their research or project meets the criteria for exemption from standard review procedures.

What is REQUEST FOR EXEMPT REVIEW (REQUIRED FOR ... Form?

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A request for exempt review is a formal application submitted to seek exemption from certain regulatory requirements or review procedures that would otherwise apply.
Generally, organizations or individuals conducting specific types of research that meet certain criteria, such as minimal risk to participants, are required to file a request for exempt review.
To fill out a request for exempt review, individuals should complete the designated form provided by the relevant regulatory body, providing detailed information about the research project and how it qualifies for exemption.
The purpose of a request for exempt review is to determine whether a research project can be exempted from full review based on its nature and the risks involved to participants.
The request for exempt review typically requires information such as the study's title, research protocol, participant recruitment methods, informed consent process, and potential risks.
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