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Updated IRB Policies and Procedures,
10/18/2007
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The Office of Research Oversight and Compliance is pleased to announce that the updated IRB Standard Operating Policies and Procedure Manual has been added to our website. The SOP manual has been expanded to include such policies as new guidance on Adverse Event Reporting, Investigator Responsibilities, and a new format/process for Exempt studies.
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IRB Electronic Project Applications,
8/6/2007
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Electronic, on-line submissions.
The Office of Research Oversight and Compliance (or "IRB Office") is pleased to announce the adoption of the IRBNet suite of tools, bringing electronic protocol management, on-line submissions and many other important features to the Sparrow Health System research community.
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IRB Review Fees,
12/26/2006
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Effective January 1, 2007, the Sparrow Health System's Institutional Research Review Committtee (IRB), the Office of Research Complaince and Oversight, and hospital administration have established charges for the review and administration of clinical research projects.
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Human Subjects Training Requirement,
12/28/2005
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On December 11, 2006, the IRRC approved a revision to their Human Subjects Training requirement. The length of time for valid certification of Human Subjects Training has changed from one year to two years. At the end of the two-year period, all Investigators and key research personnel will be asked to submit verification of recertification of their Human Subjects Training to the IRB/Research Office.
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