| 1 x | Effective Monitoring of Medical Device Clinical Investigations | € 1’517.00 |
| 1 x | Introduction to Medical Device and Clinical Investigation Planning | € 161.00 |
| 1 x | Adverse Event Processes | € 275.00 |
| 1 x | The Clinical Investigation Plan | € 161.00 |
| 1 x | ISO 14155 – Responsibilities of Principal Investigator | € 124.00 |
| 1 x | The Informed Consent Process | € 161.00 |
| 1 x | ISO 14155 – Responsibilities of Sponsor | € 176.00 |
| 1 x | ISO 14155 – Clinical Investigation Conduct | € 160.00 |
