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- GP Workflow Assistant 283 - September 2026
GP Workflow Assistant 283 - September 2026
Updated
by Charlotte Wood
Release 283 Release Notes - September 2026
This page contains details of new and amended functionality included in the software update known as Release 283.
GP Workflow Assistant Code Suggestions now present text from letter to validate findings
(Internal Reference D10-16627)
What have we done?
When a SNOMED Code Suggestion is made the code will be presented alongside the relevant source text from the document.
Why have we done this?
To give clinical coders more information when reviewing AI code suggestions and make it easier to verify where in the document the AI has sourced its information from.
How will you benefit?
Clinical coders can now see the document text that contributed to a suggested clinical code, helping them verify the suggestion before accepting it.
Details of the change
AI Suggested SNOMED codes now include a 'found in document' section, displaying the relevant source text in italics and quotation marks so users can see which content contributed to the suggestion.
GP Workflow Assistant now identifies if Blood Pressure Readings have been found in a letter
What have we done?
(Internal Reference D10-16628)
We have improved the GP Workflow Assistant panel to identify any Blood Pressure readings found within the document.
Why have we done this?
To provide users with the ability to add a Blood Pressure codes with the correct values.
How will you benefit?
Clinical coders can now add Blood Pressure readings identified in the document.
Details of the change
A new BP Readings section shows the number of Blood Pressure readings identified in the document. Users can select the detected Systolic and Diastolic values on the letter to populate the value fields, while the event date is populated automatically and can be edited if required.
GP Workflow Assistant Medical Device Compliance Information
(Internal Reference D10-16548)
What have we done?
Added medical device compliance information to the Docman welcome page when GP Workflow Assistant is enabled.
Why have we done this?
GP Workflow Assistant is classified as a medical device, so users need to be able to see the relevant regulatory and product identification information when using the feature.
How will you benefit?
Users will have clear visibility of the regulatory status and key identification information for GP Workflow Assistant, based on the applicable requirements for their region.
Details of the change
When GP Workflow Assistant is active, the welcome page now displays the relevant medical device information, including the manufacturer, UDI-DI, GP Workflow Assistant and Docman10X software versions, and the appropriate UKCA or CE compliance marking.
This information is only displayed when GP Workflow Assistant is active.