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ClinicalTrials.gov compliance workflow for academic institutions

Results reporting, run as an operational workflow — not a scramble. Academic institutions often oversee hundreds of investigator-initiated records on ClinicalTrials.gov, and FDA's March 2026 reminder initiative — more than 2,200 sponsors associated with more than 3,000 registered trials that had not yet posted results — included publicly funded researchers. Most trackers show who's late; Eichor Academic is the workflow layer we're building for PRS administrators and research-integrity teams:

• Live institutional dashboard — every record classified (posted · window open · due soon · appears overdue), refreshed daily from public registry data
• Assignment & remediation tracking — route each late record to its PI/coordinator, track it to resolution, escalate on silence
• Board-ready reporting — one-click compliance summaries for your IRB, research council or dean's office, sealed in a tamper-evident audit ledger

Early-access pricing will be institution-friendly (a few hundred dollars a month — not an enterprise suite). Join the list and tell us what your office actually needs; early institutions shape the build.

Public registry data only. Informational — not legal advice or a compliance determination.