IRB Content

Consortium News

The SMART IRB team has published a new paper that provides background and updates on the platform and Agreement.

Excerpt from abstract:

Single institutional review board (IRB) review of multisite research increased in frequency over a decade ago with a proliferation of master IRB more

Consortium News

The revised Common Rule, released by the U.S. Department of Health and Human Services (DHHS), is the first major change to these regulations in more than 25 years. Human research protection professionals are subject to following the revised Common Rule provisions, with a compliance deadline of  more

Consortium News

Before a clinical trial can begin, an institutional review board (IRB) must determine that the study is ethical and that participants’ rights are protected. This oversight step is crucial, but it can take a long time and delay studies from starting, particularly those at multiple sites. In more

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