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Page 1 of 9 LSUHSCNO IRB#: 20047 Consent Rev. date: 03Apr2020 Protocol Revision #: 31Mar2020, v10ID#:___472020Consent to Participate in a Research Study KEY INFORMATION FOR: TREATMENT IN PATIENTS
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It is a document outlining the revised common rule for an institutional review board.
Researchers conducting studies involving human subjects are required to file revised-common-rule-ic-templatedocx - page 1.
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The purpose of revised-common-rule-ic-templatedocx - page 1 is to ensure that research involving human subjects is conducted ethically and in compliance with regulations.
Information such as study protocol, informed consent process, risks and benefits to participants, and procedures for data management must be reported on revised-common-rule-ic-templatedocx - page 1.
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