№ files_lp_4_process_3_104429
Institutional review compliance checklist outlining regulatory criteria and documentation requirements for Institutional Review Board determinations when research protocols request a waiver or alteration of the informed consent process.
Year: 2025
Document Code: HRP-410
Date: 7/11/2025
Document Type: Compliance Checklist
Subject: Waiver or Alteration of Informed Consent in Research
Related Document: HRP-314 – Worksheet – Criteria for Approval
Regulatory Context: IRB Review Requirements
Institutional Body: Institutional Review Board (IRB)
Intended Users: IRB Members and Designated Reviewers
Review Stages Covered: Initial Review, Continuing Review, Modifications, Expedited Review, Convened IRB Review
Scope: Determinations and protocol-specific findings required for approving waiver or alteration of the consent process
Applicable Regulations: FDA Regulations and Federal Human Subjects Research Regulations (including 2018 Rule references)
Content Elements: Submission information, reviewer identification, study details, regulatory criteria checklists, protocol-specific justification fields
Price: 8 / 10 USD
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