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Document contents qmsWrapper Technical Overview
  1. 1 Architecture & Module Map
  2. 2 Foundation Layer
  3. 3 Design-Cycle Layer
  4. 4 Post-Market Layer
  5. 5 Governance Layer
  6. 6 Cross-Cutting AI Capabilities
  7. 7 What Each Actor Sees
  8. 8 Why This Architecture
  9. 9 Glossary

qmsWrapper Technical Overview · Chapter 7 of 9

What Each Actor Sees

7. What Each Actor Sees

ActorWhat Wrapper shows themWhen
Employee (anyone)Notification bell + Todo list; quality-event reporter; AI Chat scoped to current page.Continuously.
TraineeTraining assignments in /todo ; PIN-sign-on-acknowledge for SOP changes.On assignment + recertification.
PRRCMTF + EUDAMED + Vigilance dashboards; PRRC appointment letter; per-device Regulatory Health Score; AI Findings inbox.Daily.
RA LeadMTF + SaMD-TF + EUDAMED + Vigilance + Submission Package Generator + NB Communication Log + AI Governance Log.Daily during submission cycles.
QMS ManagerManagement & Audit dashboard; ISO 13485 clause-coverage map; AI Findings inbox; CAPA queue; Approval queue; Audit-Readiness gauges; SOC-2 Evidence Locker.Daily.
QA ContactQES triage; CAPA stage advancement; Receiving-QC alerts; Vigilance incident classification.Daily.
Engineer / DesignerTF / SaMD-TF tabs; Traceability Matrix; Risk Log; Training assignments.Daily during development.
AI/ML LeadAI Governance Log — every system, dataset, model version, V&V run, monitoring tile.Daily.
Information Security OfficerCybersecurity Log — ISMS Doc Register, Vuln Tracker, SBOM Registry, Pentest Results, Access Control Review, SOC-2 Evidence Locker, FDA Cyber Submission Package.Daily.
Purchasing AgentSupplier Master Registry; Receiving QC; Switching & Dual-Sourcing scorecards.Daily.
Internal AuditorManagement & Audit Log + per-clause evidence drill-down; CAPA audit; Training audit; Cyber audit.Quarterly internal-audit cycle.
ExecutiveRegulatory Health Score gauges per device per regulator; Open Gaps by Regulation; Vigilance Snapshot last-30d; NB Communication queue.Weekly.
NB AuditorEvery Log filtered by audit scope; the same dashboards the QMS Manager uses; AuditSignature chain.Annual surveillance + unannounced.
FDA InspectorCAPA Log + Complaint Files + Design-Controls evidence + QMSR clause coverage + Cybersecurity evidence + AI Governance Log + AI HITL audit.FDA inspection.
MDSAP AuditorISO 13485 clause map + per-chapter evidence + Training + CAPA + Supplier + Risk.MDSAP audit.
EU Competent AuthorityVigilance Log + EUDAMED submission status + UDI Registry + DoC store.On request + per vigilance reporting.
MHRA InspectorUK MDR 2002 evidence + UKRP mandate + per-UK-device evidence + UK Vigilance.On request.
SOC-2 AuditorCybersecurity Log SOC-2 Evidence Locker (per CC# per period); Access Review records; Backup tests; Encryption inventory; Security training; Incident log.Type-2 attestation period.
ISO 27001 AuditorISMS Document Register; Risk Register; Annex A applicability statement; control evidence; Internal audit; Management review.Stage-1 + stage-2 + annual surveillance + 3-year recertification.

Frequently asked questions

What does an FDA inspector see in qmsWrapper?

During an FDA inspection, qmsWrapper shows the inspector the CAPA log, complaint files, design-controls evidence and QMSR clause coverage, alongside cybersecurity evidence, the AI governance log and the AI human-in-the-loop audit. These are surfaced for the inspection scope rather than the full daily operator view.

What does a Notified Body auditor see in qmsWrapper?

For annual surveillance and unannounced visits, an NB auditor sees every log filtered by audit scope, the same dashboards the QMS manager uses, and the audit-signature chain. This gives the auditor scoped access to the underlying evidence plus the tamper-evident signature trail proving record integrity.

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