About Reeve
The eQMS we always wanted.
Reeve is built by people who've sat on both sides of a notified-body audit. We started this because the alternatives were either six-figure enterprise platforms or a folder structure pretending to be a quality system.
The market for electronic quality management systems has a peculiar shape. At the top end you have legacy enterprise platforms with a six-figure annual price tag, a six-month implementation, and a UI that hasn't changed since the early 2010s. At the bottom you have spreadsheets, SharePoint folders, and Word templates wearing the costume of a quality system.
We think there should be a middle. A real eQMS that small and growing medical-device manufacturers can adopt in a week, that an auditor can navigate without a training video, and that doesn't make the quality manager dread Monday.
So we built one. Reeve is opinionated where the standards are opinionated (no, you cannot delete a CAPA), flexible where they aren't (your workflows, your numbering, your retention policy), and built on a stack designed for the next decade - not the last one.
What we value
How we build Reeve
Auditor-ready, not auditor-hostile
The audit trail is not a feature - it is the spine of the product. Every regulated change is signed, timestamped, and immutable. Inspections become a documentation drill, not a fire alarm.
Standards as a first-class concept
ISO 13485, EU MDR, and 21 CFR Part 11 are not labels we slap on a brochure. They are wired into the data model. SOPs link to clauses, audits cite findings against them, and reports cite back.
Fast where it matters
A quality manager spending hours fighting the system is the system's fault. We obsess over the time-to-resolved-NC and the time-to-approved-SOP, not just the time-to-first-click.
Honest about trade-offs
Some features take time. Some standards conflict with each other. We don't pretend otherwise - we ship the trade-off, document it, and revisit when the evidence changes.