Eurofins Medical Device Consulting offers customized training and courses on industry topics. Our experts enjoy passing on knowledge from their fields of expertise.
We also offer a large variety of virtual and on-site seminars, and webinars.
Our trainings and seminars focus on various topics, such as:
- Regulatory Affairs – strategic considerations, culture of compliance, executive training, etc.
- Quality Management - ISO 13485/QSR
- Biological Evaluation – ISO 10993
- Risk Management – ISO 14971
- Software Lifecycle Management – IEC 62304
- Reprocessing & Sterilization
- Medical Device Quality Systems Management – ISO 13485 (as applicable)
- Medical Device Design Control Process
- European Union Medical Device Regulation – EU MDR 2017/745
Medical Device trainings (in Italian) can be found here