FOUNDATIONS01
How medical devices are developed
A practical introduction to design controls, evidence and the product lifecycle.
PRACTICAL MEDICAL DEVICE LEARNING
Build knowledge.
Develop better devices.
Clear, role-relevant learning for the people who design, develop, verify and bring medical devices to market.
Role basedLearn what matters for your work
Standards groundedConnect requirements to practice
Evidence focusedUnderstand what good looks like
01 — FEATURED LEARNING
Start with the knowledge
you need now.
From first principles to specialist guidance, each pathway turns complex requirements into practical understanding.
STANDARD SERIES02
IEC 60601 for development teams
Understand electrical safety, essential performance and what the standard means for your work.
STANDARD SERIES03
ISO 11608 for needle-based systems
Focused guidance for engineers, verification teams, risk managers and leadership.
02 — LEARNING BY ROLE
Your role shapes
what you need to know.
Choose your discipline to find guidance written around your responsibilities, decisions and evidence.
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Engineering
Electronics, embedded software, mechanical, cloud and architecture.
Systems & V&V
Systems engineering, verification, validation and test laboratories.
Quality & Regulatory
Quality, regulatory, risk, supplier quality and post-market teams.
Leadership & Delivery
Founders, executives, product owners and programme managers.
03 — EXPLORE THE SUBJECTS
One connected
development system.
Medical device development works when the disciplines connect. Explore each subject on its own, or follow the links between them.
OUR PURPOSE
“Standards tell you what is required. Good learning helps you understand why—and what to do next.”
MedTechLearning provides structured, detailed learning and study material for medical device professionals.
For consulting support, visit pg-consulting.net ↗. For current commentary and regulatory developments, visit medtech.blog ↗.