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

Clinical Safety Case Report (DCB0160) · Approve stage

Safety case report

Oakfield Surgery (a made-up practice)

What it's for
The short summary the CSO signs to say the tool is acceptably safe to use, with the controls in place. Two to six pages is plenty.
Who
Written and signed by the CSO. The partners accept the remaining risk.
When
Before go-live. Updated after reviews and significant changes.
PracticeOakfield Surgery
Tool and versionKestrel Consult, version 4
SupplierKestrel Health Ltd
Report version and date1.0, 23/02/2026
Clinical Safety OfficerDr Helen Marsh, GP partner

1. Summary

Our conclusion in two or three sentences

With the controls in our hazard log in place, the CSO considers Kestrel Consult acceptably safe to introduce for admin and clinical requests in core hours. Five hazards were found. After controls, all are scored 2 (acceptable).

2. The tool and how we'll use it

Description and scope

Patients send requests through our website and the NHS App. Care navigators sort them; the duty doctor reviews anything clinical. In scope: adult and parent-on-behalf-of-child requests in core hours. Out of scope: video consultations and automatic booking.

3. How we assessed it

Method

Review of the supplier's DCB0129 safety case report and hazard log. A one-hour hazard workshop on 06/02/2026 with clinical and care navigation staff, including a salaried GP who regularly does duty doctor sessions, walking through a request from start to finish.

4. Main hazards and controls

Summarise. The full detail is in the hazard log.

IDHazardRisk beforeKey controls and mitigationsRisk after
H1A patient with red-flag symptoms is not directed to an urgent assessment in time3Red-flag stop on the form; duty doctor reviews symptom requests within two hours2
H2A patient whose problem needs an earlier or different assessment waits for a routine appointment3Auto-booking limited to admin and clearly routine requests; free text read the same day2
H3A patient’s request is not actioned when it needs to be, while they believe the practice is dealing with it3Symptom requests in core hours only; named queue owner; end-of-day check2
H4The right patient isn’t assessed, and decisions are made using the wrong patient’s record3Patient details checked before filing; second check for requests made on someone’s behalf2
H5A patient who can’t use the form, because of age, disability, language or no internet, is assessed later than they need to be3Same-day appointments reserved for phone and walk-in; reception can complete the form2

5. Supplier assurance

What we received and checked

DCB0129 safety case report and hazard log (January 2026), DTAC, confirmation that the product is not a medical device. The supplier's CSO is named in their report.

6. Remaining risk

Why the remaining risk is acceptable

All hazards score 2 after controls. The controls are in place and staff have been trained. The partners accepted the remaining risk at the practice meeting on 23/02/2026.

7. Conditions for go-live

Anything that must be in place first

Symptom requests in core hours only. Red-flag stop tested before go-live. Auto-booking limited to admin and clearly routine requests. Phone and walk-in route kept, with reserved same-day appointments.

8. Review

When we'll review this

After three months (June 2026), then yearly, or sooner after an incident or a significant product change.

RoleNameSignatureDate
Clinical Safety Officer
Partner, accepting the remaining risk on behalf of the practice