Two focused intelligence platforms, built around the same idea: turn complex data into decisions you can trust.
Five public registries — payments, device events, trials, publications, and facilities — reconciled into one searchable entity graph. With automated watchers for trial changes and new PubMed articles.
Record inspector measurements, validate them against your specifications and sampling standards, confirm equipment calibration, and produce audit-ready lot records — automatically.
"From public registries to production floors — one source of truth, no reconciliation after the fact." Built for medical device and quality teams working to ISO 13485 and FDA 21 CFR Part 820