Sample data. This flow isn’t wired up. Every number below is illustrative, not reported trial data.
Contribute your trial’s safety data
A sketch of how a sponsor would add harmonized safety data under a shared agreement, and what they’d get back. This is a concept; it shows the shape of the idea, not a working submission.
Map your terms
Align your adverse-event terms to the shared vocabulary. We show the mapping for you to confirm before anything is submitted; nothing is auto-accepted.
Submit under a shared agreement
Your data is harmonized the same way as every other contributor’s. No sponsor ever sees another sponsor’s private data; only pooled, de-identified aggregates are shared.
Get your comparative view
See your own trial next to the pooled picture: the same rates, denominators, and term mappings, so you can benchmark without rebuilding the dataset yourself.
What you get back
Your trial, side by side with the pooled picture.
Illustrative figures. In the real thing, every number would carry its source and denominator, exactly like the rest of this site.
How trust is kept
- • Every contributor’s data is harmonized the same way.
- • No sponsor sees another’s private data.
- • An independent group runs it; funding is capped per sponsor.
- • The methods are public; sponsors keep their own FDA/EMA duties.
These are the neutrality principles behind the concept. see the full governance model.