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.
ID: N350
14 minutes
1 modules
Learning Objectives:
- Gain essential skills to manage risk effectively throughout medical device clinical investigations, including critical processes like study suspension and early termination.
- Stay up to date on the latest thinking regarding precise adverse event categorization.
- Get acquainted with the concept of estimand and how to reach more accurate results with well thought through study design parameters.
Be the first to learn about significant upcoming changes in the standard, from minor tweaks to major shifts, and position yourself at the forefront of clinical investigation practices.
Who should enroll:
Clinical Project Managers, Clinical Research Associates, Medical writers, Investigators, study coordinators and any other party involved in clinical investigations.
Prerequisite Knowledge:
A thorough understanding of the current ISO 14155: 2020 document is essential