European Medical Devices Regulation (EU) 2017/745

Introduction to medical device regulations

Risk Management for Medical Devices per ISO 14971

IQ, OQ, PQ - Verification, and Validation for Medical Devices

Electromagnetic Compatibility and Radio Compliance for Medical Devices

IQ, OQ, PQ - Verification, and Validation for Medical Devices

Best Practices for Developing End-to-End Cloud-Powered Medical Devices

US FDA Labeling Requirements for Medical Devices

Join the Master in Medical Device Engineering

US FDA Medical Device QSR, 21 CFR 820 and Quality Management System

US FDA Medical Device QSR, 21 CFR 820 and Quality Management System