Need to Know

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. 

On Friday July 10, 2020 at approximately 8am EST Huron will be upgrading the Click IRB module and will last until approximately 8am EST Monday July 13, 2020.

The National Science Foundation (NSF) released an updated Proposal and Award Policies and Procedures Guide (PAPPG) in January 2020. The new PAPPG is effective June 1, 2020.