Spring 2013 Institutional Review Board (IRB) analyst brown bags

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 March 26, 2013, allow HIPAA authorizations for research studies to be built into the consent form in nearly all cases, even when the research has optional components. They also permit authorization for future research. This means fewer forms to submit and a more integrated process. Come learn about:

  • The changes to the regulations;
  • The new combined consent and authorization form templates; and
  • How these changes affect past, present, and future studies.

May 23, 2013: Request for determination
Led by Melinda Allie and Kaija Maggard
11:30 a.m. to 12:30 p.m. in UHS 8B60

Determining what is human subjects research and what is not can feel like a tricky process. Come discuss with the IRB Analysts why you must submit a request for determination to the IRB and gain a clearer understanding of how these regulatory-based decisions are made. Topics include:

  • Quality Assessment and Improvement v. Research
  • Human Subject v. Non-Human Subject Research
  • Case Studies
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