At DeSia, we deliver targeted training programs to strengthen your team’s expertise in medical device development, regulatory compliance, and quality management. Our courses are designed to be practical, up-to-date, and aligned with current international regulations and standards.
We offer both on-site and online training, helping you optimize costs, minimize downtime, and ensure consistent knowledge across your organization.
Training Topics Include:
- Clinical Investigations for Medical Devices
- Clinical Performance Studies for IVD
- Design Process Control
- EN ISO 14971 Risk Management
- EN ISO 13485 Quality Management Systems
- MDSAP
- MDR / IVDR Post Market Surveillance
- Clinical Evaluation for MDR
- Performance Evaluation for IVDR
- EU 2017/746 IVDR
- EU 2017/745 MDR
- Usability Engineering
Experienced industry professionals deliver all training and can be tailored to your specific device type, market requirements, and company processes.
Do you need support with training your team? Contact us for further information.