IRB Member 5th Thursday Training Details
The Office of Research Subject Protection will be hosting a workshop for IRB Members. We will host hour-long training sessions on three different topics: RAMS-IRB, Regulations (FDA, HIPAA, etc.), and Reviewing Research. We will hold each training session three different times (once during each hour-long time block). You are encouraged to choose to come to whatever training sessions you feel would be helpful in your review process, at whichever times are convenient. We hope to see you there! If you have questions, please contact Meghan Wright ([email protected]).
Location: BioTech 1
Date: March 31, 2016
Session 1: 12:00-1:00
-RAMS-IRB – BioTech 3044
-Reviews – BioTech 3060
-Regulations – BioTech 3029
Session 2: 1:00-2:00
-RAMS-IRB – BioTech 3044
-Reviews – BioTech 3060
-Regulations – BioTech 3029
Session 3: 2:00-3:00
-RAMS-IRB – BioTech 3044
-Reviews – BioTech 3060
-Regulations – BioTech 3029
- RAMS-IRB— This session will focus on the technical aspects of completing reviews using the electronic submission system, RAMS-IRB. We will walk through the process, give some quick tips/shortcuts, and address specific questions.
- Regulations—This session will focus on some of the more difficult and involved regulatory requirements encountered while reviewing submissions, such as FDA regulations, and HIPAA. We will discuss these regulations and how they impact your reviews.
- Reviewing Research—This session will address the process of effectively and efficiently reviewing a submission. We will also discuss how to best present your review at a full board meeting, including writing final reviewer notes.
Categories Uncategorized