See which NIH-funded trials may need results-reporting attention. NIH verifies ClinicalTrials.gov registration and results reporting as part of award administration, and unresolved reporting can hold up a progress report. FDAAA civil penalties for continued non-compliance can exceed $10,000 per day — a statutory maximum, adjusted for inflation and rarely levied in practice. Trial-level trackers tell you a study is late; what a research office needs is the other direction: which grants are attached to late trials, before a progress report stalls.
Informational only, from public ClinicalTrials.gov and NIH RePORTER records — not legal advice or a compliance determination. Also need the full institutional workflow (assignment, remediation, board reports)? Join the Academic early-access list →