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DPIA Addendum: Audit Evidence

This addendum supplies technical evidence for a deployment Data Protection Impact Assessment (DPIA). The deploying organisation must complete and approve its own DPIA.

Processing

The audit envelope processes identifiers, roles, authorization decisions, request context, IP addresses, affected-record identifiers, and redacted event metadata. Native exports can contain historical source payloads and require the same or stronger protection as the underlying health data.

Purpose and necessity

The purposes are patient-safety investigation, security monitoring, access accountability, incident response, support-access oversight, records management, and evidence of control operation. Ordinary HTML page views are excluded to reduce unnecessary collection.

Risks and controls

Risk Control Residual decision
Tokens or credentials enter logs Shared redaction, opaque session references, credential type/record IDs only Review new event metadata before release
Household evidence leaks Per-household chains, tenant-filtered admin view, dedicated verifier/exporter roles Restrict exported files and WORM read access
History is changed or deleted Immutable runtime grants, chained hashes, signed checkpoints, Object Lock copies Database-owner activity needs external oversight
Excessive retention Versioned schedule and retain_until; no indefinite claim Records manager/DPO approve production policy
Existing history is overstated Distinct legacy-baseline epoch and explicit limitation Preserve baseline wording in reports
Export creates another health-data copy Signed manifest and audited export to a controlled output path Deployment must define transfer and deletion handling

Required approval

The deploying organisation must document its lawful basis and access roles. It must also document the retention schedule, WORM provider and region, international transfers, data-subject handling, processor terms, incident contacts, and records-manager and Data Protection Officer approval before production use.