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Buy clinic AI with every answer in writing and no surprises after you sign

By the wai teamOctober 15, 20267 min read

Reviewed by The Wellness Clinical Team, October 5, 2026

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Key points

Summary

Before buying clinic AI, check the contract and data protection terms, the subprocessor list, where records are hosted, how clinical output is signed off, what happens to the data on exit, and whether the price is published. Get each answer in writing, with a document behind it.

Run the fifteen questions below in an afternoon and the clinic signs with a full file of written answers, ready for any regulator or auditor who asks. Each question comes from what regulators require.

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8
minimum terms a UK GDPR controller to processor contract must contain under Article 28(3) 1
53%
of US health system executives surveyed named disparate software platforms as a data-sharing barrier 4
38%
of OECD countries have no clinical standards or vendor certification for EHR systems 5

Bring this checklist to the demo and see each answer shown on the product, with the documents sent after.

Clinic AI procurement checklist
AreaWhat to ask forA good answerWarning sign
Contract rolesWho is controller and who is processor, in writingRoles named in the contractRoles left undefined
Data processing agreementThe signed DPA, checked against the 8 Article 28 termsAll 8 terms presentA generic terms of service only
US business associate agreementWhen the BAA is signedBefore any patient data is processedOffered after go-live
SubprocessorsThe current list, each with its role and agreementNamed list with notice of changesNo list, or no notice period
Hosting locationThe country where records are stored and processedThe clinic's own country, in the contractLocation not stated
Security controlsEncryption, access control and key managementStated standards and role-based accessVague assurances
CertificationsCertificates held and those in progressDocuments attached, open gaps datedBadges with no documents
Clinical sign-offWho signs notes, letters and codesThe clinician, every timeAnything sends automatically
Intended useA one-sentence intended use and device statusClear statement in writingUnable to say
Audit trailAn export of the event log from a test sessionEvery action with a name and timeNo export
Patient consent and noticesTemplate wording for patientsReady-made notice and consent textLeft entirely to the clinic
AccessibilityWCAG level of patient-facing partsWCAG 2.2 AANo stated level
Exit and exportExport format, window and deletion dateFull export, deletion confirmedExport by request only, no date
PricingPublished price, setup and usage termsPublic prices, limits agreed before billingPrice only after several calls
ReferencesA clinician who uses it dailyA live demo by a working clinicianSlides only

Answers in writing

Ask each vendor for a written answer and the document behind it, for every row. The contract terms, the US agreement and the medical device questions are all set out in public guidance, and the checklist turns that guidance into questions for one meeting.

Contract and data protection

Under UK GDPR, the clinic is usually the controller and the vendor a processor. The ICO sets out the minimum terms the contract must contain, processing only on documented instructions, a duty of confidence, security measures, rules on sub-processors, help with patients' rights, help to the controller, end-of-contract provisions, and audits and inspections.1 Ask for the data processing agreement and tick each one off.

In the US, the matching document is the business associate agreement. The HIPAA rules require it to oblige the vendor to make sure its subcontractors accept the same restrictions, and to return or destroy all protected health information at termination where feasible.2 Ask when it is signed. For wai Checkout, the BAA is signed before anything goes live.

The UK terms say a processor must not engage another processor without authorisation and must tell the clinic of intended changes so it can object.1 wai names every subprocessor, with what it does and the agreement in place, and gives thirty days notice before anything changes.6

Clinical safety and sign-off

Ask the vendor what the software is for, in one sentence, and whether it is a medical device. The MHRA asks manufacturers of software to write an intended use statement because intended purpose decides how the product is regulated.3

Then ask who signs. The clinician should review and sign every note, letter and code, and no clinical message should reach a patient without a clinician's signature. wai states that rule on its security page, alongside approval by the team for every operational message.6

Ask to see the event log of a test session. Every draft, edit, approval and signature should be visible with a name and a time, and the clinic should be able to export it.

Certifications and honest gaps

Ask which security certifications the vendor holds today, with the certificate or report attached, and which are in progress with a date. A dated list of open gaps is a good sign.

wai lists on its security page AES-256 encryption at rest and TLS 1.3 in transit, and offers each open gap with a status and a date on request.6

Exit, pricing and references

Ask for the export format for notes, letters, messages and the event log, how long export stays open after termination, and the date by which copies are deleted. The UK terms require deletion or return at the end of the contract at the clinic's choice.1

In a Deloitte survey of 30 finance leaders at large US health systems, 53% named multiple disparate software platforms as a barrier to meeting data-sharing rules.4 OECD reporting adds that 38% of member countries have no clinical standards or vendor certification for EHR systems, so the clinic makes this check itself.5

Ask for the price in writing, including setup, usage allowances and what happens beyond them. wai publishes its prices on the pricing page, and Admin starts with a demo and a 90-day pilot.7 Then ask to speak with a clinician who uses the product daily.

The checklist

Each row in the table is one question, the answer to expect and the warning sign. Filed together, the written answers become the clinic's due diligence record.

Where to start

Send the checklist to every shortlisted vendor before the demo, and ask for written answers and documents within a week. Score each row green, amber or red, and only book a pilot with vendors who have no reds.

Then agree the pilot measures before signing, using our guide to pilot success criteria, and ask each vendor where the data will sit, using our data residency questions.

Send us the checklist before the demo and get each row answered in writing and shown on the product.

Frequently asked questions

What is the single most important document to ask for?

The data processing agreement, or in the US the business associate agreement. It sets what the vendor may do with patient data and what happens to it at the end.1

Should we require SOC 2 or ISO 27001?

Ask which certifications are held, with documents, and which are in progress with dates. wai answers a vendor assessment in writing, control by control, and sends its open work on request.6

Is clinic AI a medical device?

It depends on its intended purpose. Ask the vendor for its intended use statement, which the MHRA treats as the starting point for classification.3

What should the contract say about leaving?

That the vendor deletes or returns all personal data at the clinic's choice, deletes existing copies unless law requires them kept, and gives a full export before that.1

How do we compare prices fairly?

Ask for the full price in writing, including setup, usage allowances and charges beyond them. wai publishes its prices on the pricing page.7

How long should procurement take?

For a private clinic, about two weeks. One week for written answers, one for the demo and scoring, then a pilot with measures agreed in advance.

Sources

  1. 1Information Commissioner's OfficeWhat needs to be included in the contract?Read 14 October 2026Read source
  2. 2Electronic Code of Federal Regulations, US Government45 CFR 164.504, uses and disclosures, organizational requirementsRead 14 October 2026Read source
  3. 3Medicines and Healthcare products Regulatory Agency, 2025Software and artificial intelligence (AI) as a medical deviceRead 14 October 2026Read source
  4. 4Deloitte, 2021Greater transparency and interoperability in health careRead 14 October 2026Read source
  5. 5OECD, 2023Health at a Glance 2023, OECD IndicatorsRead 14 October 2026Read source
  6. 6wai, 2026Security at waiRead 14 October 2026Read source
  7. 7wai, 2026PricingRead 14 October 2026Read source
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