In order to address the specific details and regulatory requirements present in a retrospective medical chart review, the UB IRB recently created a new Protocol template: the HRP-503R.
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.
The new institute will streamline efforts to turn groundbreaking drug research into viable treatments and medicines, bringing new companies and new jobs.
