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WAIVER OF DOCUMENTATION OF INFORMED CONSENT REQUEST NTH IR BHS#:CRC# (if applicable):DATE:PROTOCOL TITLE:PRINCIPAL INVESTIGATOR:PHONE/(DIRECT) EXTENSION:IRB CONTACT:PHONE/EXTENSION:A Waiver of Documentation
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How to fill out irb-waiver-or-alteration-of-ined-consent-for-clinical- template

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How to fill out irb-waiver-or-alteration-of-informed-consent-for-clinical

01
Fill out the IRB waiver or alteration of informed consent form with all required information.
02
Clearly state the reason for the waiver or alteration of informed consent.
03
Provide any supporting documents or information that may help justify the need for the waiver or alteration.
04
Submit the completed form to the Institutional Review Board (IRB) for review and approval.

Who needs irb-waiver-or-alteration-of-informed-consent-for-clinical?

01
Researchers conducting clinical trials or studies that involve human subjects may need an IRB waiver or alteration of informed consent in certain circumstances.
02
In some cases, obtaining informed consent from participants may not be feasible or may compromise the integrity of the study, so researchers may need to request a waiver or alteration from the IRB.

What is IRB-Waiver-or-Alteration-of-Ined-Consent-for-Clinical- ... Form?

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IRB waiver or alteration of informed consent for clinical research is a process by which the Institutional Review Board grants permission to waive or alter the requirements for informed consent in certain research studies.
Researchers conducting clinical studies that meet specific criteria set by the IRB are required to file for an IRB waiver or alteration of informed consent.
Researchers need to submit a request to the IRB outlining the reasons for requesting a waiver or alteration of informed consent, along with supporting documentation.
The purpose is to balance the protection of research participants with the need to conduct valuable research in situations where obtaining informed consent may not be feasible or may compromise the study's validity.
Researchers need to provide detailed information about the study protocol, the reasons for seeking a waiver or alteration of informed consent, and the steps taken to ensure participant protection.
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