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CHLA CHECKLIST FOR REQUIRED CONSENT LANGUAGE WHEN RELYING ON AN EXTERNAL IRB This checklist provides general instructions about how to customize the approved Reviewing/External IRBs consent form template(s)

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How to fill out chla-external-irb-consent-form-checklist

01

Start by reviewing the CHLA external IRB consent form checklist to familiarize yourself with the requirements.

02

Gather all necessary information and documents, such as the study protocol, informed consent form, and any additional materials required.

03

Fill out the checklist methodically, ensuring that all sections are completed accurately and thoroughly.

04

Double-check all information for accuracy and completeness before submitting the checklist for review.

Who needs chla-external-irb-consent-form-checklist?

01

Researchers and study staff who are conducting research at Children's Hospital Los Angeles (CHLA) and are required to obtain external IRB approval must fill out the CHLA external IRB consent form checklist.

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What is chla-external-irb-consent-form-checklist?

Chla-external-irb-consent-form-checklist is a form used to document consent obtained from external IRBs for research studies conducted at Children's Hospital Los Angeles.

Who is required to file chla-external-irb-consent-form-checklist?

Researchers and staff conducting research studies at Children's Hospital Los Angeles that involve external IRBs are required to file chla-external-irb-consent-form-checklist.

How to fill out chla-external-irb-consent-form-checklist?

Chla-external-irb-consent-form-checklist can be filled out by providing detailed information about the external IRB, the research study, and the consent obtained from participants.

What is the purpose of chla-external-irb-consent-form-checklist?

The purpose of chla-external-irb-consent-form-checklist is to ensure that proper consent is obtained from participants in research studies conducted at Children's Hospital Los Angeles.

What information must be reported on chla-external-irb-consent-form-checklist?

Information such as external IRB details, study participant consent information, and study protocol details must be reported on chla-external-irb-consent-form-checklist.

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