Explore the Learning Library →Developing a medical device
Intended purpose → Requirements → Risk → Development → Verification → Release → Maintenance
Seven linked stages, a short exercise at each step, and a standalone syringe infusion pump example covering mechanics, electronics and embedded software.
Welcome to MedTechLearning
MedTechLearning is a free educational website offering practical, accessible guidance for people involved in developing and supporting medical devices.
The material explains the intent behind requirements, the evidence expected and how different disciplines fit together. It draws on recognised standards, regulatory guidance and practical development experience.
My aim is to help you understand the work, ask better questions and develop better devices.
MedTechLearning is a work in progress. New topics and resources are being added regularly, so please check back often to see how the learning library develops.
What's New
The latest learning pathway, case study and AI modules.
View all learning →Explore the dedicated AI learning section
→MTL-142Batteries and Medical Devices
→MTL-604Professional organisations and communities
→MTL-141Designing connectivity and the extra work it brings
→MTL-140Start here: developing a medical device
→MTL-603AI in Medical-device Development and Quality Management
→MTL-602Applications of AI in Medical Devices
→MTL-408Medical AI — From Claim to Controlled Use
→MTL-509AI Security, Robustness and Adversarial Resilience
→MTL-508Generative AI and Large Language Models in MedTech
→MTL-507Post-market Monitoring, Drift and Model Performance
→MTL-506Predetermined Change Control Plans for Medical AI
→MTL-505Verification, Validation and Clinical Evidence for Medical AI
→Learn about medical devices
Choose the route that best matches what you need to understand.
Core Medical Device Topics
Understand the lifecycle, design controls, risk, verification, manufacturing and post-market responsibilities.
Explore general topics →02Learning by Role
See what medical-device development means for your discipline, interfaces, decisions and evidence.
Find your role →03Regulations, Standards & Guidance
Start with the regulatory framework, then see how standards and guidance support compliant development.
Browse regulatory learning →Independent. Practical. Evidence focused.
The content supports learning and professional discussion. It does not replace current legislation, standards, regulatory advice or your organisation’s quality-management system.