Medical Devices Course
Master the full lifecycle of medical devices for healthcare: from FDA and EU MDR pathways to ISO standards, risk management, hardware, software, cybersecurity, and clinical evaluation—so you can bring safer, compliant innovations to patients.

flexible workload of 4 to 360h
valid certificate in your country
What will I learn?
The Medical Devices Course gives you a fast, practical overview of how to define, design, and launch safe, compliant devices. Learn key US and EU regulatory pathways, ISO 13485 and ISO 14971, risk management, and essential standards. Explore hardware, software, cybersecurity, usability, clinical evaluation, and data protection so you can move from concept to approved, reliable products with confidence.
Elevify advantages
Develop skills
- Regulatory strategy: map FDA and EU MDR paths for connected medical devices.
- Risk and safety design: apply ISO 14971, FMEA and controls to wearable devices.
- Hardware and software architecture: design safe, low-power, BLE-enabled monitors.
- Verification and clinical proof: plan V&V, usability and lean clinical evaluations.
- Cybersecurity and data privacy: secure PHI with HIPAA/GDPR-aligned controls.
Suggested summary
Before starting, you can change the chapters and the workload. Choose which chapter to start with. Add or remove chapters. Increase or decrease the course workloadWhat our students say
FAQs
Who is Elevify? How does it work?
Do the courses have certificates?
Are the courses free?
What is the course duration?
What are the courses like?
How do the courses work?
What is the course duration?
What is the cost or price of the courses?
What is an EAD or online course and how does it work?
PDF Course