Stanford Medical School Irb

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Human Subjects (IRB) | Research Compliance Office

https://humansubjects.stanford.edu/

School of Medicine; Stanford University; Training. CITI (Tutorial) Presentations; Compliance Monitoring & Policies; Consent Process. Non-English Speaking Participants; …

IRB Medical Application Process | Research Compliance …

https://researchcompliance.stanford.edu/panels/hs/for-researchers/med-application

Stanford has 5 medical IRBs with monthly convened meetings, so there are IRB meetings nearly every week in most months. Notable exceptions are November and December, …

Regulatory Approvals | Research Management Group …

https://med.stanford.edu/rmg/clinical-trials/routing---approvals/irb-src.html

The study team initiates the review processes through Institutional Review Board (IRB), Stanford Scientific Review Committee (SRC) and Research Management Group (RMG) …

Overview of the IRB Application | Research Compliance …

https://researchcompliance.stanford.edu/panels/hs/for-researchers/overview-of-the-irb-application

The Protocol Director (PD) should consider the following when adding personnel: Key personnel should be listed in eProtocol, including all persons who are responsible for the …

Rosters | Research Compliance Office

https://researchcompliance.stanford.edu/panels/hs/rosters

Stanford has eight IRBs, seven that review medical research and one that reviews non-medical research. At Stanford, the IRBs are formally known as Administrative Panels for …

Medical Research: Forms & Consent Templates

https://researchcompliance.stanford.edu/panels/hs/for-researchers/forms-templates/medical

Medical Research: Forms & Consent Templates. *Please note that when creating a protocol for IRB submission, these investigators need to select the Medical eProtocol Application …

Charges | Research Compliance Office

https://researchcompliance.stanford.edu/panels/hs/policies/charges

The charge emphasizes that the IRBs are functionally independent and have ready access to the highest officials, if needed, to ensure protection for human research participants. …

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