“How to Submit Initial Protocols” will cover everything you need to know about submitting a new initial application for IRB review. This session will focus on the substance of an IRB application rather than technical elements of the eIRB platform. Presenters will focus on submission requirements for both clinical and social-behavioral research including what to […]
“Ongoing Submissions” will focus on post-approval IRB submissions including amendments (modifications), continuing reviews, deviations, reportable events, exception requests, annual check-ins, and closures. Presenters will define each submission type, discuss when they are needed, and review what they should include. This session will focus on the substance of each submission type with brief overviews of how […]
Video Conferencing/Human Research Protections Program Office of the Institutional Review Board 3600 Civic Center Blvd, 9th Floor
“Informed Consent 101” will review expectations for obtaining consent from participants in biomedical and social-behavioral research. Content will include required elements of consent, HIPAA authorization, tips for making consent a process rather than an event, and criteria that need to be met for alterations and waivers of consent to be approved. This session is relevant […]
Video Conferencing/Human Research Protections Program Office of the Institutional Review Board 3600 Civic Center Blvd, 9th Floor
Video Conferencing/Human Research Protections Program Office of the Institutional Review Board 3600 Civic Center Blvd, 9th Floor
Video Conferencing/Human Research Protections Program Office of the Institutional Review Board 3600 Civic Center Blvd, 9th Floor