Cyrille Lefèvre has been working on the optimization of end-to-end clinical supplies with N-SIDE for more than 8 years. He has experience advising both large and small pharma for the forecasting and optimization of their clinical trials for all phases and through multiple therapeutic areas. Cyrille also has extensive experience training teams focusing on strategic planning and improving IRT resupply algorithms and the way they are used.
Learn about the latest advances in clinical trial forecasting and optimization. Understand how technology can help you overcome challenges you face in your clinical trial supply management.Read now
With a growing global population, speeding up drug development timelines is of paramount importance for all pharmaceutical and biotech companies. Thanks to innovative software solutions it’s now possible to make better decisions at each stage of the clinical supply chain.Download now
As trials become more global and protocols and therapeutics become more complex, clinical trial timelines are getting longer. Learn about the main bottlenecks delaying clinical research and discover ways to deal with them and speed up drug development timelines.Read now