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Click on the logo below to log into UConn's Qualtrics site. An IRB staff member screens the IRB-3 form and, if applicable, the protocol, consent form or material required for submission for completeness and corresponds with the PI by e … Passwords are not stored in IRIS for network accounts. Use your UConn Health network ID and password to log in. The research involves a one-time anonymous survey (either in person or online). Submission of … Investigators will seek IRB Waiver of the requirement that participants must sign the consent form. If you have any questions concerning your rights as a research participant, you may contact the University of Connecticut Institutional Review Board (IRB) at 860-486-8802.”] [For international studies, rather than provide participants with the IRB Office phone number, give participants the general IRB e-mail address – irb@uconn.edu For example an IRB number of 19-001C-2 reflects receipt of the study in fiscal year 2018/2019, that it was the first study received within the fiscal year and that UConn Health is the IRB for Connecticut Children’s Medical Center, and that the submission was reviewed by Panel 2. Babbidge Library Compliance Forms (IRB, IACUC, FCOI, IBC, SCRO) Interfaith Religious Calendar NIH Office of Extramural Research Office for Human Research Protections Policies and Procedures UConn Office of Vice President for Research Laptops will be loaned on a temporary basis. Introduction All key study personnel listed on an IRB application or request for modification must complete training in the protection of human subjects. If you have any questions concerning your rights as a research participant, you may contact the University of Connecticut Institutional Review Board (IRB) at 860-486-8802.” [For international studies, rather than provide participants with the IRB Office phone number, give participants the general IRB e-mail address – irb@uconn.edu. The Hartford HealthCare (HHC) Institutional Review Board (IRB) is supported by the Human Research Protections Program (HRPP). If a study meets criteria #1 but does not meet criteria #2, the researcher will need to use the appropriate Waiver of Documentation of Informed Consent Template. documents, available in the Researcher’s Guide section of the IRB website, be reviewed before answering the questions. Also, IT Loaner Laptop RequestDirectors, Deans and Department Heads can submit the IT Loaner Laptop Request Form to request loaner laptops for staff in their departments who do not have appropriate technology to work remotely. Courses offered through the Collaborative IRB Training Initiative (CITI) are the primary mechanism used to satisfy this requirement. If you still need help, M-F from 9 - 4:30 contact Mayra Cagganello (679-8802, cagganello@uchc.edu) or Deb Gibb (x3054, gibb@uchc.edu). The HHC IRB has oversight over all research conducted at HHC, including research conducted at Hartford Hospital; MidState Medical Center, Windham Hospital, The Hospital of Central Connecticut (HOCC), and Backus Hospital. 8.4.2020 Notice from Qualtrics: Click here Technical support: Qualtrics Academic Support Qualtrics FAQ's: Click here for PDF To transfer ownership of surveys and non-technical questions: natalka.tuczkewycz@uconn.edu IRB questions, processes, and forms: Office of the Vice President for Research • IRB-1 or IRB-9 Word document study protocol form (always download current version from IRB website) • Appendix A (list of key personnel) online eform • Data Security Assessment Form (always download current version from IRB website) Other essential documents for IRB submission that may be relevant to your research • Consent form(s) A PI may amend his/her approved protocol by submitting an IRB-3 Amendment Review form. 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