SR&ED for medical devices.
Medical-device work combines engineering uncertainty with regulatory rigour, and much of the experimentation behind it is SR&ED-eligible. The documentation you already keep for compliance often doubles as claim evidence.
What qualifies in Medical Devices & Health Tech?
Eligibility comes down to one test: did your team work through genuine technical uncertainty? In medical devices & health tech, that usually looks like this.
- Device design and iteration
- Verification and validation testing
- Solving biocompatibility or materials problems
- Developing embedded software or algorithms
- Experimentation driven by regulatory requirements
What a claim looks like
A device startup iterated a sensor design that kept failing validation at temperature.
A health-tech company developed an algorithm to cut false positives below the required threshold.
A manufacturer solved a biocompatibility issue by developing and testing a new material.
How Chrono builds your claim
Chrono reconstructs defensible, evidence-linked timesheets and technical narratives from the records you already keep. No manual time tracking required.
- Design history files
- Git history
- Test and validation protocols
- QMS records
Medical Devices & Health Tech, answered
Is regulatory testing SR&ED?
The experimentation needed to meet requirements can be. Routine compliance testing against a known standard isn't.
Our product is software-only. Do we qualify?
Yes. Algorithm development and systems work for a health product can qualify on the same basis as any other software SR&ED.
See what your Medical Devices & Health Tech claim is worth.
Estimate your credit in two minutes, then let Chrono build the claim from the data you already have.