Gerard Sanderink
Vice President Laboratory Sciences Sanofi
Seminars
Thursday 25th September 2025
Impact of IVDR & IDE/LDT Regulations on Patients’ Timely Access to Drug-Diagnostics Clinical Trials
10:00 am
- Streamlining global clinical trials to meet regulatory demands depending on location
- Introducing efficient strategies to manage and reduce the complexity and volume of approval applications within the European regulatory environment
- Comparing IVDR and IDE
