Medical device
development,
without the drag.
Mosaic is a purpose-built platform that folds regulatory compliance into everyday execution — so teams design, document, and commercialize faster, with far less friction and a great deal more agility.
The premise
Today, compliance happens after the work. Documentation gets reconstructed. Design history becomes archaeology.
Every submission becomes a fire drill. It is a tax paid twice — once in the months spent assembling evidence of what you did, and again in the speed you gave up doing it.
We think that’s backwards. The record should be a consequence of the work, not a project of its own.
Mosaic is being built by people who have shipped regulated products and have opinions about why it takes so long.
What we’re building
Compliance by construction
Regulatory evidence accrues as a byproduct of the work your team is already doing. Nothing is reconstructed after the fact, because nothing was ever missing.
One system, not two
Engineering execution and design controls live in the same place. No parallel universe of documents shadowing the real work, drifting a little further out of date each sprint.
Velocity without exposure
Traceability that keeps pace with iteration. Move at the speed the product demands and stay audit-ready on any given Tuesday.
Get in touch
We’re quiet, but we’re listening.
We’re in stealth and working closely with a small number of device teams. If any of this sounds like a problem you have, we’d genuinely like to hear from you.
Prefer email? hello@mosaicmedtech.com