Secure SAR response.
On time. Every time.
Secure SAR response.
On time. Every time.
Coordination at every stage of the SARs lifecycle through orchestration, automation, and governed AI. While maintaining human review and
staff control.


Increasing SAR Volumes
As legislation and NHS guidance continue to evolve, organisations must be prepared to manage increasing operational demand and complexity.

More Complex Requests
Modern SARs increasingly require clinical review, serious harm assessments, third-party considerations and complex disclosure decisions.

Information Fragmentation

Regulatory Scrutiny
Failure to meet statutory Subject Access Request obligations can result in ICO investigations, reprimands and enforcement action, placing organisations under increased regulatory scrutiny.
What Our Solution Provides
SIGNIFICANT REDUCTION IN
CYCLE TIME
Significant Reduction in
Cycle Time
Well over 75% achievable depending on the amount of human effort removed.
REDUCTION IN
COLLATION AND BUNDLING ERRORS
Reduction in Collation
and Bundling Errors
Fewer mistakes, less rework and higher quality redaction packs every time.
REDUCTION IN THE TIME
TAKEN TO REDACT DOCUMENTS
Reduction in the Time
Taken to Redact Documents
AI technology can auto redact and facilitate human approval. Staff can add new redaction criteria and the model learns.
DELIVERING COMPLETE AND
COMPLIANT RESPONSES
Delivering Complete and
Compliant Responses
All SARs resolved in statutory timeframes, improving compliance and reducing escalation risk.
ROI CAN BE DELIVERED
WITHIN YEAR 1 OF DEPLOYMENT
ROI Can Be Delivered
Within Year 1 of Deployment
Measurable return through reduced manual effort, improved efficiency and lower operational cost.
MORE TIME FOR
SPECIALIST WORK
More Time for
Specialist Work
Reduces administrative workload, enabling governance teams to focus on clinical judgement and complex cases.
Governed Connected Workflow

