Stanford Medical Irb

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Human Subjects (IRB) | Research Compliance Office

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

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

STARR Tools | STAnford Research …

https://med.stanford.edu/starr-tools.html

The STARR IRB permits the collection and aggregation of all data generated at Stanford for clinical care purposes, and articulates the formal approval process each research …

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 …

Regulatory Approvals | Research Management Group …

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

The Principal Investigator (PI) is responsible for assessing and addressing all applicable regulatory approvals for the study. The study team initiates the review processes through …

Single IRB (sIRB) | Research Compliance Office

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

Relying on a Single IRB (sIRB) Stanford's IRB may agree to rely on a single IRB (sIRB) for multisite studies to provide initial and ongoing regulatory reviews. The reliance terms are …

Non-Medical IRB Application Process - Research …

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

The IRB members represent a variety of disciplines. This means that some reviewers will not be as familiar with the terminology as you are, so please use language that a lay person …

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