Explore the Learning Library →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
Eight most recently published topics.
View all learning →Principles and Practices for Medical-device Cybersecurity
→ MTL-318Software as a Medical Device Principles and Clinical Evaluation
→ MTL-317EU Post-market Surveillance, PMCF/PMPF and PSUR Guidance
→ MTL-316Clinical and Performance Evaluation of Medical Device Software
→ MTL-315MDCG Medical-device Cybersecurity
→ MTL-314Software Qualification and Classification
→ MTL-313FDA Interoperable Medical Devices
→ MTL-312FDA Changes to Existing Devices and Software
→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 → 03Standards & Guidance
Navigate the standards, regulations and authoritative guidance that shape development work.
Browse standards →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.