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In the second part of a two-part series, “Research Roundtable” highlights additional elements of the “Study Registration” FAQ section from ClinicalTrials.gov.
ClinicalTrials.gov has an extensive FAQ section ranging from general to investigation-specific. This edition of “Research Roundtable” highlights a selected FAQ, “Study Registration.”
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.
Dr. Mabry and the panelists talk about programmatic interests, funding opportunities, and resources on systems science at NIH at a webinar held for an audience at University of Buffalo.