WebDec 20, 2024 · Research Education Series. “Learn More about the Research Offices” Office of Sponsored Programs Publications Poster Presentations Office of Human Research Protection (IRB) Clinical Trials Management Office Legal Affairs. Navigating the Grants Process at GHS. Slideshow 9196523 by... WebIf you have any questions after reviewing the tutorials below, please contact the eIRB Help Desk at 410-502-2092, or email [email protected] for further assistance. If you have a specific question about the review of a protocol (e.g. timeline for review, questions about how to respond to issues raised by the Board, etc) contact a staff member ...
Onboarding Checklist for Clinical Research Professionals (CRPs)
Web8 rows · HSSC’s eIRB is a web-based, paperless system for IRB submissions, review, and management. eIRB supports initial applications, tracking, and routing of all submission … REDcap is a self-service tool available for surveys as well as data acquisition, … WebPermanently set your Home Organization. On this page, you can set a default Home/AffiliatedFigure 1 - Local Administrator's Screen Showing Pending and Current … ata hotel
School of Nursing - University of South Carolina Aiken
WebSep 1, 2024 · This study was approved by the Prisma Health Institutional Review Board (IRB; eirb.healthsciencessc.org; protocol #Pro00057182) and was registered with Clinicaltrials.gov (NCT04950088). Written informed consent was obtained from all participants. A prospective randomized analysis was completed at a single outpatient … WebAfter signing into this site, you are bound by the Terms of Service and Privacy Policy set forth when you received your account. WebFollow these steps to add or edit a study status in Velos. From the Summary page, click the Study Status tab. Click Add a New Status. Select the Organization, Status Type, IRB. Select Study Status of Submission Initiated. Select today’s date. Enter your e-Signature in the e-Signature field (default is “1234”) and click Submit. fuszekli fehernemu