Answer questions about conducting human subjects research. Provide guidance and answer questions about the electronic application forms in the HawkIRB system. Provide suggestions and guidance about study procedures that are in compliance with federal regulations and the UI IRB policies. Provide guidance and answer questions about the submission of industry-initiated and industry-sponsored research projects to an external/commercial or central IRB.

Office Hours: IRB Office Hours are for all UI faculty, staff, and Investigators, HawkIRB delegates, and research team members involved with Human Subjects research. No appointment necessary.(make sure this is the correct link for the semester). First come, first served; computers are available. HSO Staff will be available to: Answer questions about conducting human subjects research. Provide guidance and answer questions about the electronic application forms in the HawkIRB system. Provide suggestions and guidance about study procedures that are in compliance with federal regulations and the UI IRB policies. Provide guidance and answer questions about the submission of industry-initiated and industry-sponsored research projects to an external/commercial or central IRB.

This presentation will clarify the key aspects of ClinicalTrials.gov registration and results reporting, with an overview of guidelines and practical tips to avoid common errors that researchers encounter during this process. By the end of this presentation, participants will have a clear understanding of how to meet the Food and Drug Administration Amendments Act (FDAAA 801) standards and ClinicalTrials.gov requirements, ensuring successful trial registration and reporting.

Answer questions about conducting human subjects research. Provide guidance and answer questions about the electronic application forms in the HawkIRB system. Provide suggestions and guidance about study procedures that are in compliance with federal regulations and the UI IRB policies. Provide guidance and answer questions about the submission of industry-initiated and industry-sponsored research projects to an external/commercial or central IRB.