Showing results for IRB

Our organization is going to be a sIRB (or central IRB, or CIRB, or primary site in a multi-site trial), how do we give them access to CITI?
The organization serving as an sIRB would purchase a separate CITI Program annual subscription for sIRB purposes.  The account would be named “Orga...

Does CITI Program work with electronic submission systems used by IRBs and IACUCs to provide access to learner data?
Yes, CITI Program can usually be integrated with these third-party protocol management systems for an additional fee. Our technical team can provide m...
Pragmatic Clinical Trials: What Hospitals and IRBs Need to Know
Presented by: Stephanie Morain, PhD, MPH - Johns Hopkins University; Challace Pahlevan-Ibrekic, MBE, CIP - Northwell Health  Learning Objectives: ...
Safety Reporting to Regulatory Agencies and Institutional Review Boards (IRBs)
This module extends the analysis from prior modules to describe how different federal agencies, such as the U.S. Food and Drug Administration (FDA) an...
IRB Protocol Review
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