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
The master lifecycle plan for AI/ML-enabled medical devices, integrating the IEC 62304 software lifecycle, the IMDRF Good Machine Learning Practice principles and the Health Canada 9-stage ML lifecycle. It sets the framework that every other AI document in the kit references. Fully editable Word template, built from public primary sources.
€69.00
Alessandro Stella
Alessandro Stella is a freelance Medical Device Regulatory Consultant and ISO 13485 / ISO 9001 Lead Auditor based in Italy. With over 13 years of experience spanning R&D, Quality, and Regulatory Affairs, he has supported companies across Europe and beyond in EU MDR technical documentation, QMS implementation, ISO 13485 compliance, and FDA submissions. His device expertise covers cardiovascular devices, AI-based standalone software, robotic surgery systems, active wearables, and more. Alessandro is the founder of MD Regulatory.