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
Gerard Sanderink