Healthcare, aged care and disability providers | Australia-wide

AI Consulting for Healthcare Providers

Clinicians lose hours to notes, letters, referrals and reporting. We help health organisations take that load off with AI, while keeping patient information inside the rules that govern it: the Privacy Act, TGA medical device regulation and AHPRA's expectations of practitioners.

Why Health Is a Harder Place to Use AI

Most of the AI tools now sold to practices do something useful. An ambient scribe drafts the consult note, a document tool reads incoming referrals, a reporting agent pulls numbers out of the practice management system. The difficulty is everything around the tool. Health information is sensitive information under the Privacy Act 1988, and the OAIC is clear that the Act applies to every private sector health service provider whatever its size or turnover. Recording a consultation and sending it to a vendor is a collection and a disclosure, so consent, notice and where the data goes all need answers before go-live.

Then there is the TGA. Software, including AI, is regulated as a medical device when its intended purpose is diagnosis, prevention, monitoring, prediction, prognosis or treatment. The TGA's guidance gives the example of a digital scribe that starts outside the definition and moves inside it once the developer adds diagnosis or treatment suggestions. Features change with every vendor update, so a tool that was administrative when you bought it may not stay that way. Our TGA software as a medical device guide explains where the line sits.

Finally, AHPRA's guidance confirms that practitioners remain accountable for anything AI contributes to the record or to a decision. The AHPRA AI guidance post sets out what that means day to day.

Who This Work Suits

We qualify by the problem in front of you. A single clinic and a multi-site group can have the same one.

Documentation backlog

Clinicians finishing notes, letters and reports after hours, or referrals sitting in an inbox waiting to be keyed in.

A scribe or AI tool under evaluation

A vendor demo looked good and you need someone to check data flows, consent and the TGA position before you sign.

Systems that do not talk

Practice management, billing, rostering and reporting in separate systems, with staff copying data between them.

Sector reporting obligations

Aged care, NDIS or accreditation reporting assembled by hand from several sources each cycle.

Shadow AI in clinical teams

Staff already pasting patient details into public chatbots because nothing approved exists yet.

Microsoft 365 with patient files

Clinical or HR documents in SharePoint and Teams, with Copilot on the roadmap.

If patient files live in Microsoft 365, start with our Copilot readiness assessment, because Copilot answers from whatever each user can already open. For the public chatbot risk, see how the wrong AI tools leak business data.

What the Engagement Includes

Use case screening

Each candidate use case is checked against its intended purpose, the TGA definition of a medical device and the APPs that apply to the data it touches. Administrative use cases with clear value go first.

Data flow mapping

For every tool, we document what is captured, where it is processed and stored, whether it leaves Australia, how long it is retained and whether the vendor trains on it.

Process automation

Referral intake, correspondence, recalls, claims paperwork and reporting, built with a clinician or staff member approving anything that reaches a patient record. See our process automation service.

Integration

Connecting practice management, finance and reporting systems so data is entered once. Our system integration work covers the APIs and the access controls around them.

Private deployment options

Where contracts or policy require in-country processing, we design self-hosted models inside your environment through our private AI infrastructure service.

Governance and consent

Patient notices, staff AI use policy, review steps for AI-drafted notes and an incident path, aligned to the AHPRA guidance and your privacy policy.

Related services: process automation, system integration and private AI infrastructure. Background on hosting choices is in our data sovereignty guide.

See what this would take in your business

A free 30-minute review on Microsoft Teams. Bring the process you want fixed and leave with a clear first step.

Book your free review

A First Screen for Any Health AI Tool

Where Does This Tool Sit?

What is the tool intended to do?
Booking, recalls, billing, correspondence
→ Administrative: privacy and data flow review
Record and summarise a consult for the clinician to check
→ Administrative today: watch vendor updates for scope creep
Suggest diagnoses or treatments
→ Likely a medical device: confirm ARTG inclusion
Predict deterioration or triage risk
→ Likely a medical device: confirm ARTG inclusion

This screen is a starting point and does not replace a regulatory determination. Intended purpose is set by the manufacturer's own claims, so we read the vendor's materials alongside the product. Where the answer is unclear, the TGA accepts questions and pre-submission meetings, and we recommend you use them.

What You Receive

  • A use case register ranked by value and regulatory weight, with the TGA and Privacy Act position noted for each.
  • Data flow maps for each shortlisted tool, including overseas disclosure and vendor training terms.
  • A pilot design with a defined cohort, review steps for AI output and baseline measures taken before go-live.
  • Draft patient notice wording and a staff AI use policy for your privacy officer and clinical lead to approve.
  • A build or buy recommendation, and where we build, working automations handed over with documentation.

How a Healthcare Engagement Runs

1
Phase 1
Discover
Interview clinical, admin and privacy leads, list systems and pain points, collect vendor documents
2
Phase 2
Screen and map
Regulatory screen per use case, data flow maps, shortlist
3
Phase 3
Pilot
One administrative use case with a small cohort, human review and measured baselines
4
Phase 4
Scale and govern
Extend to more teams, finalise policy, set a review cycle

Timeframes depend on how quickly vendors answer data handling questions, so we set them after discovery. Engagement options are on our pricing page, and if you have not yet settled on priorities, our AI strategy service is the place to start.

When We Are the Wrong Fit

  • You want to build and sell a diagnostic or treatment AI product. That needs a regulatory affairs specialist and a quality management system, which we do not provide.
  • You need clinical advice on whether a tool is safe for patients. That judgement belongs to your clinicians.
  • You only need calls answered at the front desk. Our healthcare industry page covers that separately.
  • You want AI in place this week with no review of data flows. We will not skip that step with patient information.

For front-desk call handling, see healthcare practices. For a wider view of the obligations covered here, read Privacy Act compliance and AI, our post on aged care AI under the new Act and the guide to NDIS registration and automation. Once tools are live, our managed AI services keep the review cycle running.

Frequently Asked Questions

Talk Through Your First Use Case

Book a 30-minute scoping call. Bring the process that costs your clinicians the most time and any tool you are already evaluating, and we will tell you what we would check first.