| 1 x | The Clinical Investigation Plan | € 161.00 |
| 1 x | Adverse Event Processes | € 275.00 |
| 1 x | Introduction to Medical Device and Clinical Investigation Planning | € 161.00 |
| 1 x | Effective Monitoring of Medical Device Clinical Investigations | € 1’517.00 |
| 1 x | Managing Data Release Consent During Post Market Studies | € 75.00 |
| 1 x | Ethics Committee(EC) / Institutional Review Board Requirements | € 143.00 |
| 1 x | EU-MDR 2017/745 Review for Clinical Professionals | € 234.00 |
| 1 x | Good Documentation Practices for Clinical Study Files | € 161.00 |
