← All templates
Download WordExample (Word)

Draft for review by a Clinical Safety Officer. Adapt it to your practice before use.

DPIA (UK GDPR Article 35) · Assess stage

Data protection impact assessment (DPIA)

Oakfield Surgery (a made-up practice)

What it's for
Records what personal data a tool uses, why it's lawful, the risks to people's privacy, and what you've done about them.
Who
Practice manager drafts it with the supplier's help. The DPO advises. A partner, as SIRO, accepts the remaining risk.
When
Before the tool is used with personal data. Reviewed when use changes, and at least yearly.
PracticeOakfield Surgery
Tool and supplierKestrel Consult, Kestrel Health Ltd
DPIA version and date1.0, 18/02/2026
Completed byJo Reid, practice manager
Data Protection OfficerOur DPO service

1. Why we need a DPIA

What the tool does and why a DPIA is needed

Patients send requests, including health information, through our website and the NHS App. This is new technology processing special category data about many patients, so a DPIA is required.

2. The data

Follow the data from start to finish. Ask the supplier for their data flow diagram, or draw your own as boxes and arrows, then list each flow in the table.

#From → toWhat movesHow
1Patient → toolThe request: symptoms, any photos, name, date of birth, contact detailsOnline form on the website or NHS App, encrypted
2Tool → Heron Link → EMISName, date of birth and NHS number to find the patient, then the requestHeron Link, another company, runs the link
3Tool → staffThe requestStaff log in to the tool; access by role
4Staff → EMISNotes, codes and actionsTyped by staff, who open the patient in EMIS separately
5Staff → patientThe replySent from the tool by text or email to the contact details given
QuestionAnswer
Whose data?Registered patients, and parents or carers acting for them
What data?Name, date of birth, NHS number, contact details, the request including symptoms and any photos
Where does it come from?Patients, through the online form. Reception enters phone requests.
Where is it stored, and in which country?Supplier's cloud servers in the UK
Who can see it?Care navigators, clinicians and the practice manager, by role. Supplier support staff only when we ask them to help. Heron Link, the integration partner that links the tool to EMIS, passes details through but doesn’t use them.
Is any of it shared or sent on?Relevant parts are copied into the GP record. Nothing else is shared.
How long is it kept?In the tool for 90 days after the request is closed, then deleted. The record keeps what matters.
Does the supplier use it for anything else, such as training AI?No. The contract rules this out unless the data is anonymised.
How many people?About 9,000 registered patients; around 900 requests a month

3. Is it lawful?

QuestionAnswer
Our roleController. The supplier is our processor.
Lawful basis (UK GDPR Article 6)6(1)(e): a task in the public interest, providing NHS care
Condition for health data (Article 9)9(2)(h): providing health care
ConfidentialityUsed for direct care, so implied consent applies. Patients are told in our privacy notice.
Data processing agreement in place?Yes, signed 10/02/2026
Supplier's DSPT statusStandards Met, 2025-26

4. Who we asked

Who was consulted and what they said

DPO (advice below). Caldicott Guardian: content with the access controls. Patient participation group: asked for clear guidance on what to put in the form. Supplier: provided their DPIA, hosting details and DSPT.

5. Is it necessary and in proportion?

Do we need all of this data? Could we do it with less? How do we tell patients and support their rights?

The form asks only for what's needed to handle the request. Free text is needed for clinical requests. The privacy notice and website explain the tool. Patients can still phone or call in. Rights requests are handled through our usual process.

6. Risks to people's privacy

For each risk, score likelihood (remote, possible, probable) and severity (minimal, significant, severe) to give an overall rating (low, medium, high). The clinical risks go in the hazard log, not here.

RiskLikelihoodSeverityOverall
Staff add notes or send a message to the wrong patient because the tool and EMIS don’t open the same patientPossibleSignificantMedium
A reply reaches someone other than the patientPossibleSignificantMedium
Heron Link, the integration partner, handles patient details when linking the tool to EMISPossibleSignificantMedium
Too many staff can read requestsPossibleSignificantMedium
Data is stored outside the UKRemoteSignificantLow
The supplier uses requests to train or improve its productPossibleSignificantMedium
Requests are kept longer than neededProbableMinimalLow

7. What we're doing about them

RiskMeasuresResidual riskApproved?
Wrong patient open in EMISCheck name, date of birth and NHS number in both systems before adding or sending; close each record when finished; wrong-record entries corrected and reported as a data breachLowYes
Reply reaches the wrong personCheck who the reply goes to before sending; sensitive replies ask the patient to phoneLowYes
Integration partner handles dataNamed as a subcontractor in the supplier’s agreement on the same terms; UK storage; DSPT completedLowYes
Too many staff can readAccess by role; access log checked monthlyLowYes
Stored outside the UKUK hosting written into the contractLowYes
Supplier reuses dataContract rules it out unless anonymisedLowYes
Kept too longDeleted 90 days after closingLowYes

8. Sign-off

ItemName and dateNotes
Measures approved byJo Reid, 18/02/2026
Remaining risk accepted by (SIRO or partner)Dr Helen Marsh, 23/02/2026All residual risks low
DPO advice givenDPO service, 16/02/2026Add retention period to privacy notice
DPO advice accepted or overruled?AcceptedIf overruled, say why
Caldicott Guardian consultedDr Tom Hughes, 12/02/2026
Next reviewJune 2026, then yearly

If a high risk remains that you can't reduce, you must consult the ICO before you start. Your DPO will advise.