| 1 x | Source Document Verification | € 108.00 |
| 1 x | Deviations and Non-Compliance Handling | € 54.00 |
| 1 x | Adverse Event Processes | € 275.00 |
| 1 x | ISO 14155:2020 - Responsibilities of Principal Investigator | € 125.00 |
| 1 x | Clinical Evaluation Report: Review for Regulatory Professionals | € 308.00 |
| 1 x | The Case Report Form Process | € 161.00 |
Update ISO 14155 version DIS 2024 - Free Summary
Update ISO 14155 version DIS 2024 - Free Summary
Gain early insights into the anticipated ISO 14155 updates with our FREE SUMMARY presentation by Danielle Giroud.
Discover key changes in risk management, clinical investigation protocols like suspension and early termination, and clearer adverse event categorization.
The standard is still in a draft format and hence changes may still happen. However, the overall changes described in this presentation will provide you with a preview of what is coming next year.
1 modules