ReproTrack is a Medical Device Reprocessing compliance platform for Ontario cosmetic surgery clinics. It logs every sterilization cycle, every biological indicator, every high-level disinfection run, every package integrity check; it seals each day cryptographically; it produces inspector-ready evidence bundles with offline-verifiable signatures.
The reason it exists is narrow. Cosmetic clinics in Ontario are inspected by three different bodies — CPSO, MOHLTC, and Public Health Ontario — and the cost of a failed inspection runs five-figure consultant fees, potential fines, and operational disruption. Existing tools sell you a digital logbook and call it compliance. ReproTrack is built around the moment that actually matters: inspection day.
The product was shaped through conversations with practicing Medical Device Reprocessing technicians who run the workflows on the clinic floor, and with the supervisors and clinic managers who own competency sign-offs and audit prep. Every feature shipped is something a clinic asked for or a premortem identified as a real risk; nothing in the codebase is speculative or generic.
ReproTrack stores no Protected Health Information. The records are about the clinic's processes — what was sterilized, by whom, in which cycle — not patient identities. That keeps the threat model focused on audit integrity instead of patient privacy, and lets the product make stronger guarantees about what its records prove.
The platform is Ontario by design today. One regulatory framework, one inspector regime, one reference set of standards (CSA Z314) — the focus lets us go deeper rather than wider. We're actively iterating on the surfaces that would carry the product into British Columbia, Alberta, and other provinces; each adds its own inspector regime and regulatory framework, so we're building those expansions deliberately, not all at once.