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
Learning modules, worked examples and practical exercises added or updated in the last two weeks.
View all learning →Measuring Medication Adherence: From Dispensing Records to Injection Events
→MTL-606Choosing and Validating Injection-Tracking Technologies
→MTL-607Building the Evidence Case for Digital Medication Support
→MTL-331Software Integration and System Testing
→MTL-330Software Unit Verification and Testing
→MTL-103User Needs and Design Inputs — new practical exercise
→MTL-114Medical-device Risk Management — new practical exercise
→MTL-116Verification and Validation — new practical exercise
→MTL-144Practical Auditing for Medical-device Development
→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.