Collect the sample
Location, bottle, and custody stay together from the tap to the lab.
A Water OS lab and compliance module. A person still signs the report.
Water Quality and Regulatory is the lab and compliance module inside Water OS. It keeps the bottle, the result, and the report on one record. A person still signs.

Samples waiting, holding time at risk, results to review, and the next DMR — on one board.
Location, bottle, and custody stay together from the tap to the lab.
Instrument import, method, QC, and a person who reviews before it counts.
DMR, CCR, LCR, and PFAS deadlines use the same reviewed result.
Who collected it, when, and where it went stay attached.
AI can flag a QC issue.
The regulator can follow the sample to the number you signed.
Select a screen to explore the workflow. Open it for a closer look.
Leaders see sample status, exceptions, deadlines, program coverage, and report evidence from one Water OS operating record.
Plans, routes, samples, custody, instrument import, result review, and QC charts.
Limits, exceedances, Lead and Copper Rule, PFAS, TCR, DMR, CCR, and deadline tracking.
AI can flag an anomaly or draft a QC review.
The lab, the plant, and the compliance calendar often live in three systems. This module keeps the sample, the QC, and the deadline on the Water OS record so you are not rebuilding the story the week the DMR is due.
In the product this is the lab and compliance module inside Water OS: samples, QC, and regulatory reports. It can work above an instrument or an existing LIMS. A person still releases the result.
The value is keeping the bottle attached from the tap to the signed report.
Keep source context available as the workflow moves between teams and applications.
TwinEdge Water Quality and Regulatory
No. It is the lab and compliance module inside Water OS: samples, QC, and regulatory reports on the same plant record.
No. It prepares the report from reviewed results and tracks the deadline. A person still signs and submits.
No. AI can flag a QC issue or mark a result for review. Approve and reject stay with a person. High-confidence bulk approve is still a person clicking approve.
Sampling and custody, QA/QC, exceedances, Lead and Copper Rule, PFAS, TCR, DMR, CCR, sanitary surveys, and deadline tracking — using the same sample record.
Discuss your sources, assets, and the outcomes your team wants to improve.