Need to Know

Registering a study with ClinicalTrials.gov is a necessary step for investigators to be compliant with regulations. This video offers useful insights for using the Protocol Registration and Results System, as well as additional helpful resources.

If you are conducting a Human Clinical Research Study that involves services at Erie County Medical Center, Kaleida Health, Great Lakes Cancer Care Collaborative, or General Physician, PC, your study will be registered in the Clinical Research Management System.

How can you receive IRB approval without a completely fleshed-out study? Learn how to submit a Just-in-Time submission in Click to receive an IRB approval that has been accepted by NIH and NSF.

All human research studies conducted by personnel affiliated with the University at Buffalo must be submitted to the Institutional Review Board (IRB) for review and approval.

Food and Drug Administration (FDA) warnings could result in civil monetary and other penalties to investigators who fail to report results on ClinicalTrials.gov.

UB's Clinical Research Office looks behind the curtain of the Central Study Registration system and Click modules in the first edition of “Research Roundtable.”

On Friday Ausust 27, 2021 at approximately 12:30pm EST though Saturday evening Click will be unavailable due to scheduled maintenance. 

The Office of Management and Budget (OMB) has revised sections of Uniform Administrative Requirements, Cost Principles, and Audit Requirements for Federal Awards (Uniform Guidance) located in title 2 of the Code of Federal Regulations (2 CFR part 200), originally implemented on December 26, 2016.