AI for Medical Device

Hands-on AI training for medical device manufacturing teams.

Scored exercises built on medical device manufacturing scenarios, from a nonconformance to a 90-day pilot.

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Length: One day
Delivery: In person, instructor-led, trainees in pairs on shared iPads
Exercises: 5
Status: Built, first cohort pending

What you practise.

Consult the AI quality engineer

An overnight nonconformance is on your desk. Scope containment, choose the data to pull, weigh patient risk and reach a disposition you could defend to an auditor.
The CAPA investigation copilot

Six field complaints in five weeks with the same symptom. An AI agent proposes a root cause and CAPA scope; accept, narrow, widen or reject it, with reasons.
Drift on the line: stop or ship?

A parameter is trending towards its limit and an AI monitor says carry on with more sampling. Production wants to ship. Commit to a recommendation you can defend.
Audit-ready AI: device history record red flags

An AI assistant pre-filled a device history record from line data. Find the red flags an auditor would find, from out-of-sequence entries to missing second checks.
Your 90-day AI pilot

Pick a real pain point in your value stream, build the 90-day pilot you would propose, with return, roadmap and risks, then pitch it.

Who should attend.

Quality
Regulatory
Engineering
Operations
Validation

What you leave with.

A co-branded certificate
A full course record of every decision and score
An alumni code to keep practising for 12 months

See the certificate and course record

Delivery and dates.

We run cohorts at your site, on our iPads, with our instructor.

For a cohort at your own site or on your institute's instance, book a demo and we will plan it with you.

For manufacturing sites Read the evidence

Questions about this course.

Do trainees need to know anything about AI before the course?

No. Most trainees on the flagship course have never had a conversation with an AI model before the first exercise, so that exercise is an open conversation with no mark. The course starts from the work trainees already do.

Does it work without a GMP suite?

Yes. The course runs in an ordinary classroom, and a physical GMP suite is not required.

What does each trainee leave with?

A co-branded certificate, a full course record of their decisions and scores, and an alumni code to keep practising on their own device for 12 months.

Does the course certify EU AI Act compliance?

No. No course can certify EU AI Act compliance, and we do not claim to. The course builds the practical AI literacy that Article 4 of the Act asks organisations to ensure in their staff.

Bring one cohort. See the record they leave with.