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Part two in a series of articles highlighting frequently asked questions to comply with results reporting for ClinicalTrials.gov includes guidance on the Quality Control review process, protocol and statistical analysis plans, and appendices. (See part one here.)
In the second part of a two-part series, “Research Roundtable” highlights additional elements of the “Study Registration” FAQ section from ClinicalTrials.gov.
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.