Compliance that gets out of your way.
The software we wished we had: lab, quality, manufacturing, and warehouse on one login, quiet enough that your team forgets it is running. Built for the bench, trusted by the auditor.
Throughput · 14 days
samples/dayResult outcomes
Built to adapt to your regulatory regime: 21 CFR Part 11 · ISO 17025 · ISO 13485 · ISO 9001 · GxP
How we run compliance →We were tired of software that felt like chains, not tools. So we built the opposite.
The big names are expensive, dated, and so unintuitive that techs and scientists lose half the day fighting the tool instead of doing the work. We had lived that, so we built the system we wished we had: one that stays out of the way, keeps the lab and the quality system talking to each other, and hands the bench back to the science. It is where the names come from. Vapor and Fluid: software light enough you forget it is running.
The whole result flow, in a few taps.
At the bench, one scan pulls up the sample and everything it needs, and you enter every result in a single pass, no peeling off a glove to type a password mid-run. Verification and the certificate pick up from there. The design target: 70–90% fewer clicks per result, and 2–5 hours a day handed back to a high-volume lab.
- 1Scan a sampleOne barcode scan, no menu-diving with gloved hands.
- 2Scan-and-prepVapor returns the sample and every pending test in a single call.
- 3Enter every result at onceAtomic bulk entry: all-or-nothing, no half-saved batches.
- 4Two-person verifyA verifier who is not the creator signs. The record locks.
- 5Certificate issuedA branded, versioned Certificate of Analysis, generated.
Lab, compliance, and manufacturing. One platform.
Start with the product that hurts most, or run the whole operation. Everything shares one login, one audit trail, and one set of lots, so a result, a deviation, a batch, and a shipment stay connected without exports.
Intake to a signed certificate, at bench speed.
A quality system that keeps itself inspection-ready.
Batches and stock that account for themselves.
One kernel under every product: login, signatures, trail.
Every change, attributed and immutable.
Who, what, when: captured on every change and locked once signed. When an auditor asks how a number came to be, the answer is already written. The audit becomes the easy part.
Audit trail · Result R-8842
- 1Open any recordEvery record that matters carries a history that cannot be edited after the fact.
- 2Who, what, whenEach change is attributed and time-stamped for you, with nothing to log by hand.
- 3The reason, on the recordThe §11.10(e) context an auditor asks for is already written before anyone asks.
Know where the lab stands today.
Turnaround slipping, CAPAs aging, pass rates drifting: you catch it while you can still do something about it, instead of finding out from a month-end spreadsheet.
Turnaround trend
Volume by category
CAPA aging
days openEvents by type
Start with one product. Add the next when it earns it.
Every DLBD product stands on its own, and none of them forces you into the rest. Add another later and it switches on beside what you already run: same login, same audit trail, nothing to re-enter and no migration to dread.
What usability-first compliance buys you.
See it running. Today.
Walk a real sample from intake to Certificate of Analysis, then close a CAPA with a signature an auditor will accept. All in your browser.