Covers the master programs in Microengineering and Robotics, minors in photonics and biomedical technologies, industry perspectives, and career opportunities in the medtech industry.
Explores European regulations for medical devices, covering classification, manufacturer's role, post-market follow-up, and essential requirements compliance.
Explores the regulation of medical devices in Europe, covering market authorization, risk classification, conformity assessment, and post-market surveillance.
Discusses designing electrochemical interfaces for protein immobilization and implantable devices, exploring the concept of enhanced human beings through RFID microchips.
