About AI Test Group
AI Test Group is a managed testing service for clinical software companies. We run the testing and produce the compliance evidence as a by-product of running it.
Who we are
Every engagement is run by people who understand the product and the evidence question in front of it. Not a queue of tickets handed to whoever is free, and not a template filled in after the fact.
We test the thing you actually built, in the way a reviewer will eventually read it, so the pack you end up with is a record of work that happened, not a document written to look like it did.
20+
Years in regulated systems
2
Primary compliance frameworks
Our leads
Every engagement is run by people who understand the product and the evidence question in front of it.
Founder and CEO
Helping health tech founders ship safer software without hiring a QA or compliance team.
I'm the founder of AI Test Group and ClinVerify, built around one specific problem: regulated health tech companies need to prove their software is safe, for investor due diligence and assurance reviews, but most can't justify hiring a full QA team or a compliance lead at Series A.
Head of Engineering
Head of Testing
Clinical Safety Lead
Head of Infrastructure
Business Relationship Manager
How we work
The pack is the record of tests that were actually executed against your build, not a description of tests we intend to run.
We focus the testing on product context, clinical workflow, risk controls, lifecycle evidence, and the review route in scope.
Every result is tied to the build it came from, so a reviewer can tell which version of the product the evidence describes.
Findings come to you as they surface, in language your product team can act on, not held back for a report at the end.
What clients get from us
Good evidence work is not only about a final pack. It is about having the right questions asked at the right point in product work, and keeping the answer connected as the product changes.
We agree the product version, review question, meaningful journeys, and working assumptions before execution begins.
We test against the real build, collaborate around findings, and keep the record close to the people making release decisions.
We organise the outputs so product, clinical safety, quality, and technical reviewers can understand what happened without rebuilding the story.
Book a 20-minute scoping call. We’ll look at where your evidence sits today, tell you what a Compliance Sprint would cover, and come back with a proposal within one working day.
