Register for this workshopThis online workshop discusses data management and risks/benefits ratios in human subjects research and further guidance on how to communicate those in your IRB application. Participants must have completed IRB Basics: Part 1 to attend.Instructor: Yael Allen
Register for this workshopThis online session will guide researchers on participant-centered study design related to implementing surveys and the compliance related IRB issues that should be addressed. We will cover:Survey recruitment methods including email and social mediaSampling frame uses and screening processes and how to describe that in the IRB applicationSurvey delivery modes: online, in…
Register for this workshopDoes your research involve the use of information collected for a reason other than your proposed research project? This online session will benefit both new and seasoned researchers regarding using secondary data and communicating that with the IRB. Researchers will learn how to articulate their use of secondary information as research data, including…
Register for this workshopThis online session will detail information about devices and FDA regulations and when they apply.Topics in this session include:Discussions regarding studying the safety and efficacy of a deviceDiscussion of significant/nonsignificant risk devicesDiscussion of IDE, Abbreviated IDE, and IDE ExemptionUse on label or off labelDetail PI obligations should the FDA regulations applyIRB processes…
Register for this workshopThis online session will help researchers using qualitative methods design participant-centered research and communicate their qualitative research endeavors to the IRB. We will cover:Research approaches: phenomenology, grounded theory, case study, ethnography, autoethnography, and narrative inquiryResearch data collection modes: interviews, focus groups, observations, photovoice, and surveysRisks to primary and third party participants and…
Register for this workshopThis online session will discuss the use of “off the shelf” apps and software and “homegrown” apps and software when used in research with human subjects.Attendees in this session will learn about and discuss:How to describe the app/software when used as a tool for data collectionHow to describe the app/software when it’s…
Register for this workshopThis online workshop provides a basic overview of IRB history and operations. It is designed for individuals with little to no background in human subjects research practices at NC State University and serves as a foundation for all other IRB workshops offered through the NC State University Libraries, including the IRB Basics:…
Zoom join link:https://ncsu.zoom.us/j/91943209418The Research Education and Training Team proudly hosts this live training opportunity. Beginning March 1, the Office of Contracts and Grants will transition submission and review of over 90-Day HR cost transfer actions to the new E-Retroactive Adjustment Form (RAF) process. After this date, submissions will no longer be accepted via redistribution@ncsu.edu. Come to…
Register for this workshopThis online session will go through the eIRB application question-by-question and provide targeted guidance for how to fill the application out and how to upload supporting documentation and what documents to upload. This session will focus on how to fill out the eIRB application for qualitative, quantitative, and clinical trials research; biomedical…
Preregister to attend webinar by March 3.