Melissa Cortvriendt
Join us at the BSMA Conference in Foster City in June!
The N-SIDE team will be attending the BSMA Conference in Foster City, on June 22-23. Come by our booth and meet our Life Sciences experts to learn all you need to know about streamlining your end-to-end clinical supply chain and our optimization software, the N-SIDE Suite!
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WHEN? June 22-23 | Starting time: From 7:30AM PDT
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WHERE? The Crowne Plaza Suites, Foster City, CA
On Day 1 at 4PM, Cyrille Lefèvre, N-SIDE Senior Expert, will be giving a presentation during the plenary session on:
"How to ensure that clinical supplies is a true enabler of faster clinical development timelines"
Attend our talk and you'll learn:
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How cross-departmental decision-making in the clinical trial supply, protocol design and upstream manufacturing saves time, drug, costs and ensures all patients are treated at all times;
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Through case studies, the reasons why the supply chain is one of the key enablers of faster time to market, with a 2-6 months acceleration in a program.
On Day 2 at 9:15AM, join the clinical supply chain track session and attend a panel discussion about:
Clinical Supplies Planning : Stochastic and deterministic approaches
At this roundtable, Cyrille Lefèvre and other industry experts will share their experiences and perspectives on the value, pros and cons of different tools and approaches for clinical supply planning.
We are looking forward to connecting with you!
We are giving out a few free passes! If you want to join us at the Conference, click below and fill in the form. We'll get back to you shortly. Hurry up as we only have a limited number of passes!
Speaker
Article
Forecasting and optimization in clinical trials
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.
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White paper
End-to-end clinical supply chain optimization helps bring drugs to market faster
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
Article
Drug development timeline acceleration strategies for clinical operations
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.
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