TestResults
PlatformPricing
MEDICAL DEVICE SOFTWARE TESTING

Release on the date you promised without last-minute surprises

Your dry runs are manual, partial, and take weeks. Bugs show up in formal verification. Fix, re-test, re-document, delayed launch. Again.

With TestResults, you can run your dry runs with automation. Nothing installed on your medical device. Out-of-the-box audit-ready documentation. Make formal verification literally just formal.

AUTOMATED MEDICAL DEVICE SOFTWARE TESTING

If your dry runs were thorough, formal verification would be a formality

Your current challenges

Hard to impossible to automate

Your medical device is locked down. No agents, no instrumentation. Most automation tools need exactly that. So you have to test manually.

Bugs in formal verification

Manual dry runs take weeks, so they're done partially. Bugs slip through to formal verification and the design history file.

Slow documentation, broken traceability

More time documenting than testing. Evidence scattered, requirement mapping breaks with every change.

With TestResults

Zero intrusion. Full automation.

TestResults connects via the remote access already on your device. Nothing installed, nothing changed. Your device stays untouched.

Formal verification is pure formality

Run automated dry runs after every change, as often as needed. Walk into formal verification with the assurance that you haven't missed a bug.

Full traceability, zero manual work

Tests are documented traceable, revision-based, and with evidence by default and linked back to your requirements.

Your release date should be a fact, not a hope

Run dry runs early. Run them often. No more last-minute surprises.

Manual dry runs are the bottleneck in every release cycle. They take weeks, cover only part of your risk, and happen too late to prevent issues. Run automated dry runs early, after every change, with full coverage. Formal verification becomes a confirmation, not a discovery mission.

Reliable launch schedule

With automated and thorough dry runs, your release date becomes predictable. No last-minute discoveries, no shifting the launch. The date you set is the date you ship.

80+% risk coverage

With TestResults risk-based testing aligned with your FMEA scores, you cover 80% of your risk with only 20% of your test cases. Less effort, better coverage, faster cycles.

Faster time-to-market

Automated dry runs cut weeks from every release cycle. No more waiting for manual rounds. No more re-work after last-minute bugs. Your device reaches the market faster.

Built for regulated medical devices

TestResults is built for regulated environments. FDA (21 CFR Part 820), MDR, IEC 62304, ISO 13485/14971. Every test run generates the evidence your auditor needs, automatically.

Zero intrusion

Nothing is installed on your medical device. TestResults connects via VNC or RDP. Your device integrity stays intact, your validation status unaffected.

Full traceability

Every test is mapped to requirements. Every run is logged, timestamped, and versioned. From requirement to test result, the chain is complete and auditable.

Visual evidence for every step

TestResults captures what happens on screen at every step of the test. Your auditor sees exactly what was tested, what the result was, and when it happened. Full audit trail, no manual documentation.

Your device is part of a system. Test it like one.

Your medical device doesn't work alone. It connects to a management platform, exchanges data with other devices, generates reports, triggers workflows. Testing the device in isolation misses what breaks in between.

TestResults tests the full process. From device screen to platform to documentation. Automated.

Make your releases predictable again