Clinical reporting
Clinical Report Builder for Labs
ReportStudio gives lab staff a drag-and-drop builder with template versioning, approval workflows, and a 21 CFR Part 11 audit trail. Pipeline output maps straight into the report, the software is customized to a lab's templates, and it runs on-premise. Report changes in days instead of months. The sign-off stays with the lab.
A section change should not take a developer and three months
In many labs, every new report type, panel update, or change in regulatory wording requires a developer ticket and a three-to-four-month cycle. Lab staff has no direct control over the tool they depend on every day, and without an approval step in between, an unapproved template or an unsigned report can reach a clinician. That last point is a real accreditation risk, because an amended report has to supersede every prior version and reach every clinician who saw it, which is almost impossible to guarantee without enforced versioning and sign-off.
What ReportStudio includes
ReportStudio arrives as a working report builder that a lab shapes to its own templates and rules.
- A drag-and-drop canvas for composing report layouts with no code
- A reusable component library for sections, disclaimers, and result blocks
- Direct mapping of pipeline output into report placeholders, with no copy-paste step
- Full template version history, so every change is tracked and reversible
- An approval workflow that stops any template reaching production without sign-off
- A 21 CFR Part 11 audit trail for every template and every report
What's ready to run, and what the lab tailors
The builder, the versioning, and the compliance controls already exist, so a project starts around the halfway mark rather than at zero.
| Already built | Customized for the lab |
|---|---|
| Drag-and-drop builder, component library, versioning, approval workflow, audit trail | The report templates and branding, the approval roles and rules, the pipeline-to-placeholder mapping, integrations |
Because that foundation is in place, NonStop estimates a build reaches production 40 to 50 percent faster than starting from scratch, and the lab owns the result when the engagement ends.
At the end of the workflow, owned by lab staff
ReportStudio takes approved interpretation output and turns it into a signed, compliant report that lab staff control directly.
| Receives | Approved results from interpretation (Varion) |
| Maps | Pipeline output directly into report placeholders |
| Enforces | Versioning, approval, and a 21 CFR Part 11 audit trail |
| Deploys | On-premise or private cloud |
From a developer cycle, down to a lab-staff task
| Developer-led reporting | With ReportStudio |
|---|---|
| 14–16 weeks of engineering time per report | 1–2 weeks for lab staff to build and publish |
* Figures are NonStop estimates and vary by engagement scope.
The expert sign-off stays exactly where it belongs, with the lab director or clinical geneticist who takes responsibility for the report.
Frequently Asked Questions
Can lab staff change reports without a developer?
How does it keep reporting compliant?
Does pipeline output flow into the report automatically?
Is ReportStudio an off-the-shelf product?
Can it run on-premise?
Book a call
Put your reports back under lab control
Book a 15-minute scoping call and bring a report type the lab changes often. We will show how versioning and approval would work and what the team would own.
Book a call →