Board Findings Report
Plain-English leadership summary explaining what was found, why it matters, the top risks and what should happen next. Written for non-technical readers.
Clinical AI Exposure Diagnostic™
Nine outputs. Three audiences. One evidence pack.
In four working days you receive a complete board-ready evidence pack structured for three distinct audiences: the board and senior leadership, the DPO and clinical governance team, and the insurer, MDO or CQC inspector who may ask what AI is in use and how it is controlled.
Plain-English leadership summary explaining what was found, why it matters, the top risks and what should happen next. Written for non-technical readers.
Single-page board-level visual showing Red, Amber, Green and N/A status for each AI tool across seven governance dimensions. Designed for board minutes.
Sequenced actions with named owners and required evidence to move from unmanaged to managed AI use within 30 days of delivery.
Master register of declared and shadow AI tools: owner, users, purpose, patient-data involvement, approval status and review priority for each.
High-risk indicators, DPIA status, RoPA and privacy notice gaps, retention and data-flow issues structured for DPO review and decision.
Per-tool evidence status against supplier assurance, data protection, patient transparency, clinical safety and human oversight expectations. Where applicable.
Per-supplier tracker covering DPAs, data residency, sub-processors, retention, training-data use, security assurance and international transfer indicators.
Governance evidence relevant to insurer renewal questions, MDO indemnity discussions and PMI provider due-diligence requests. Disclosure templates included.
Every finding mapped to ICO, CQC, NHS England, MHRA and MDO published guidance, so reviewers can see exactly which expectation each gap relates to.
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deliverables
Fixed fee £4,500–£6,500 + VAT. Four working days from completed intake. Senior-led delivery by Faisal Ali, CISM, CRISC. Includes a 60-minute board readout.
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