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Comment Showing 13 courses for medical devices.

Syllabus Library Detail View Calendar View
Course Quarter Units Fall Winter Spring Summer
Post-Market Regulatory Obligations for Medical Devices 1.5
Medical Device Process Validation 2.0
Value-Added Quality Audits 1.5
Global Medical Device Submissions and Strategy 1.5
Quality Management Systems for Medical Devices: ISO 13485 and FDA Requirements 3.0
Design Control for Medical Devices 2.0
Regulation of in vitro Diagnostics in Europe and the US 2.5
Validating Software for Medical Devices and Emerging Technologies 2.0
Mobile Health, SaMD, and AI/ML Devices 1.0
Risk Management for Regulated Industries 3.0
Human Factors and Usability in Medical Device Development 2.0
European Medical Device Regulation: Clinical Evaluation and Post-Market Surveillance 3.0
Mobile Health: The Evolving Industry and Regulatory Landscape None