We are seeking available supplies of N95 masks, gloves, long-sleeve Tyvek gowns, face shields, goggles, and other personal protective equipment (PPE) for UF Health clinician needs going into the COVID-19 epidemic.
COVID-19 is a significant challenge that will continue to impact our research on campus and across the state in the weeks ahead. Given the progression of impact on campus and across the state, please take the following actions immediately: Research activities that can be accomplished remotely should move to that…
The U.S. Food and Drug Administration has issued guidance for industry, investigators and institutional review boards conducting clinical trials during the coronavirus (COVID-19) pandemic. For more information, see https://www.fda.gov/regulatory-information/search-fda-guidance-documents/fda-guidance-conduct-clinical-trials-medical-products-during-covid-19-pandemic.
NIH recognizes the significant effects that the COVID-19 emergency is having on NIH-funded clinical trials and other human subjects studies.
UF is temporarily closing access for in-person monitoring visits and scheduled meetings by clinical study sponsors.
While the university is requiring that all classes be moved online, there are currently no restrictions or limitations on research activities. Access to research facilities remains unchanged for faculty, staff, graduate students and others who are engaged in these activities.
The UF OnCore Support team has created a library of user guides that include web-based step-by-step instructions, tip sheets with screen shots, and demo videos. The OnCore User Guides can be found on the OnCore Support website. For computers not on the UF Health network, VPN…
New statement messages have been added to Research Statements to assist RBO staff as they follow up on aging research accounts.
Each library in OnCore has a CTSI Biorepository management group (formerly named Pathology). Adding the CTSI Biorepository management group to a study’s list of management groups on the Management tab allows the CTSI Biorepository staff to: Verify IRB approvals for that studyVerify study subject consent/enrollmentConfigure the OnCore protocol so that samples can be recorded Study Team…
OnCore customers can use Task Lists to track a study's progress through the OCR submission.
