We provide training and support services to ensure your team is well-equipped to handle all aspects of medical device development and regulatory compliance.
Now it is in your hand to decrease the total training cost per employee by organizing an in company training and save time for all your team.
Get a proposal now for technical training your team needs.
- Clinical Studies and MDR
- Change Management
- Control of Design Process
- EN ISO 14971 Risk Management & MDR
- MDR QMS (ISO 13485) & MDSAP
- PMS, PMCF, Vigilance in MDR
- Clinical Data Assessment for MDR / IVDR
- EU 2017 / 746 IVDR Basic Information
- Usability
- EU 2017 / 745 MDR Basic Information
- EU 2017 / 745 MDR GSPR
- OEM - OBL Manufacturer (MDR)
- EN ISO 13485:2016 QMS
Please contact us to get further details on training topics or for any other technical training that is not on the list.
