AI Development & Lifecycle Plan (AI-01)
€69.00
ISO 13485 & MDSAP Ready
Editable Word & Excel
ISO 13485 / MDSAP / FDA QMSR
Used by 100+ quality teams
What it is
the master AI/ML lifecycle plan that every other document in the kit references. Integrates the IEC 62304 software lifecycle, the IMDRF Good Machine Learning Practice principles and the Health Canada 9-stage ML lifecycle into one coordinated framework that serves five regulatory markets from a single source.
What it covers
- Lifecycle phases and deliverables mapped to IEC 62304
- GMLP principles allocated across the lifecycle
- Health Canada 9-stage ML lifecycle alignment
- Roles, responsibilities and stage gates
- Cross-references to every other document in the kit
Format
One fully editable Microsoft Word document. Built from public primary sources (IEC 62304, IMDRF GMLP, Health Canada guidance). Multi-jurisdictional requirements integrated as inline notes. Instant download after purchase.
Part of the kit
This document is one of 10 in the AI/ML Medical Device Documentation Kit. Buying the complete kit (€499) instead of the 10 documents individually (€690) saves ~28% and adds the README and Excel Master Index.
€69.00


