Due to a change in the HIPAA Privacy Rule, the Institutional Review Board has revised its consent and authorization templates so that all informed consent and authorization elements are combined into...
May 23, 2013 Presented by: Melinda Allie and Kaija Maggard 11:30 a.m. to 12:30 p.m. UHS 8B60 Determining what is human subjects research and what is not can feel like a tricky process. Come...
Federal requirements dictate that studies and repository protocols be reviewed by the IRB annually. Continuing Review Questionnaires (CRQs) should be submitted at least 8 weeks prior to the...
Led by Andrea Johnson April 25, 2013, 11:30 a.m. to 12:30 p.m. in UHS 8B60 New HIPAA regulations and guidance, which take effect on March 26, 2013, allow HIPAA authorizations for research studies...
The interactions between eCoI and eIRB The new conflict of interest reporting system housed in Big Brain, eCoI has been up and running since late August. This system asks researchers to report...
April 25, 2013: The new and improved HIPAA research authorization process Led by Andrea Johnson 11:30 a.m. to 12:30 p.m. in UHS 8B60 New HIPAA regulations and guidance, which take effect on...
Quality improvement or research? How to make sure you're in the clear In the era of quality improvement, questions about how to make QI into scholarship come up frequently. FAQs about Quality...
Thursday, March 28, 2013 OHSU Hospital, 8B60 Presenter: Trish Lindstrom The Institutional Review Board (IRB) is responsible for evaluating a study to determine, among other things, whether risks...
Repository Refresher or “I got my repository approved…now what??” Andrea Johnson Thursday, February 28, 2013 at 11:30 a.m. in UHS 8B60 What happens with those stored data and specimens...
Continuing review is the ongoing monitoring mechanism by which Institutional Review Boards (IRBs) ensure the continuing protection of subjects who participate in research. The questions below, which...