The National Institutes of Health (NIH) recently initiated email notifications to administrative authorities at research institutions that have study records that are not compliant with ClinicalTrials.gov regulations.
In August 2022, the NIH implemented a series of changes to its internal procedures to ensure that scientists are complying with requirements to register studies and submit study results to ClinicalTrials.gov.
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.
The new institute will streamline efforts to turn groundbreaking drug research into viable treatments and medicines, bringing new companies and new jobs.
