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Research Roundtable: HRP-503R Retrospective Medical Chart Review Protocol Template
3/29/23
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.
UB to create AI systems to help kids with speech, language disorders
1/9/23
The $20M NSF-funded institute will address the nationwide shortage of speech-language pathologists.
Research Roundtable: NIH Email Notifications for Clinical Trials Compliance
12/12/22
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.
Research Roundtable: NIH Implements Changes to ClinicalTrials.gov Procedures
10/4/22
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.
Research Roundtable: Updated HRP-502 Consent Template - Summary of Changes
5/17/22
Beginning July 1, the UB IRB will require all new study submissions in Click to use an updated Consent Template.
Research Roundtable: 'ClinicalTrials.gov: How to Register Your Trial' (Video)
2/14/22
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.
Research Roundtable: Billing Compliance and the Clinical Research Management System
1/12/22
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.
Research Roundtable: Just-in-Time (JIT) Submissions to the IRB
12/11/21
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.