WebStarting Your Study. The sponsor of the trial will provide the relevant study materials to the Emory investigator. When the trial is investigator-initiated, the Emory investigator will need to obtain the written information on the drug/device and is responsible for the development of the written protocol and informed consent forms. http://ila.emory.edu/majors-minors/resources-for-students/current-majors/irb.html
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Web3. Decide which Emory approvals you need to obtain (see CTAC Guidebook Appendix 1) and complete applications • IRB submission via eIRB for Emory IRB or Form A/B for Western IRB (visit www.irb.emory.edu for WIRB eligibility requirements) • OCR submission for studies with billable items and services WebUsers with an Emory or Emory Healthcare NetID can log into eIRB using their NetID and password. Old eIRB: Once you log in, your account will be created automatically. New eIRB: phoenix cb radio
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WebConcomitant Medication Log; Delegation of Authority Log; Device Accountability Log; Eligibility Criteria Checklist; Enrollment Log; Informed Consent Form Version Tracking Log; ... Emory University Clinical Trials Audit and Compliance 1599 Clifton Rd. Suites 5.104 and 5.105 Atlanta, GA 30322 WebJan 21, 2024 · Emory & Henry is committed to protecting the rights of and ensuring the safety of human subjects participating in research conducted by faculty, staff and students. The IRB reviews human subject research projects according to three principles of the Belmont Report: first, minimize the risk to human subjects (beneficence); second, ensure … WebJan 18, 2024 · IRB at Emory Qualitative Research Getting Started Finding Qualitative Resources, Workshops, & Conferences Exploring Qualitative Methods Data Sets, Data Management, and Data Citation IRB at Emory Searching Tips and Citing Sources IRB Approval at Emory If you are working with human subjects, you'll need to obtain IRB … phoenix caterers