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- Human Animal Research Compliance Office
The Stanford Institutional Review Board (IRB) consists of 7 Medical Panels and 1 Non-Medical Panel Research involving Stanford Medical School personnel is reviewed by one of the Medical IRB Panels with some exceptions
- Overview of the IRB Application - irb. stanford. edu
Please see Stanford consent assent templates If you are planning to obtain consent verbally or online, select ‘ Waiver of Documentation ’ as the consent type
- Stanford University Research Compliance Office (RCO) and IRB
The RCO is responsible for oversight and management of Stanford’s Administrative (Compliance) Panels (Human Subjects (IRB), Stem Cell Research Oversight (SCRO), and Laboratory Animal Care (APLAC)) and ensures compliance with applicable policies, accreditation standards and external regulations
- IRB Medical Application Process - irb. stanford. edu
Before a research protocol can be submitted to the IRB, investigators must first identify the appropriate form type (Medical or Non-Medical) and the appropriate review type, i e , whether the protocol qualifies for Exempt, Expedited or Regular review
- Do I Need IRB Review? | Human Animal Research Compliance Office
The Stanford IRB is responsible for all human subjects research projects conducted by Stanford-affiliated researchers Projects that meet the regulatory definitions of ‘ research’ or ‘clinical investigation, and ‘ human subject’ must be submitted to the IRB for review and approval
- Getting Started with Single IRB (sIRB) | Human Animal Research . . .
The Single IRB team facilitates obtaining the Stanford signatory official’s signature on behalf of the study team The reliance agreement is signed after Stanford receives and completes its review of the 'Stanford Relying' application in eProtocol
- Regulations Policies | Human Animal Research Compliance Office
IRB Frequently Asked Questions Clinical Trials and Human Subject Protections - Guidance, resources, good clinical practices (GCPs) Human Tissue Intended for Transplantation Human Cells, Tissues, and Cellular and Tissue-Based Products FDA Tissue and Tissue Product Q A OHRP: Office of Human Research Protections Title 45 CFR 46: Protection of
- Guidance A-Z | Human Animal Research Compliance Office - irb. stanford. edu
Guidance A-Z NOTE: If you are having trouble accessing these documents, please ask IRB Education (email or call 650-724-7141) to have them sent to you Use "Ctrl+F" to search this page
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