Webinar: Understanding the benefits of risk-based optimization on clinical trial supply planning

“Risk-Based Optimization Or Clinical Supply Forecasting? The Impact On Clinical Trial Supply Planning” Our webinar at a glance: Clinical supply optimization and clinical supply forecasting are often confused with one another, but mixing up the two approaches can bring dangerous results when managing a clinical supply chain. Clinical trial optimization that is risk-based delivers many […]

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Join N-SIDE at the Clinical Trial Supply Chain Strategy Meeting!

Join N-SIDE at Proventa International’s Clinical Trial Supply Chain Strategy Meeting 2020.  WHEN? 18 November, 2020  WHERE? This is an Online Event Do not miss N-SIDE’s Life Sciences Director Sébastien Coppe leading a roundtable discussion on “Trial design: how to get clinical supplies a seat at the table?” His roundtable will be in the Technology & […]

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Optimize clinical trials manufacturing with lot sizing

Lot sizing in clinical trials manufacturing can save more than you think! Manufacturing lot sizes are often considered as a given constraint when it comes to planning clinical trials manufacturing campaigns for active pharmaceutical ingredient/drug substance (API/DS) and drug product (DP) of most clinical programs. During the planning of clinical trials manufacturing, the main scenarios […]

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Join N-SIDE at IQPC Exchange’s Clinical Trial Supply Forum!

On August 25th, N-SIDE’s Life Sciences Director Sébastien Coppe will be a speaker at IQPC Exchange’s Clinical Trial Supply Forum! Don’t miss the opportunity to learn more about N-SIDE’s solutions and strategic services for clinical trial supply chain forecasting and optimization, which every day solve challenges in clinical supply chain. WHEN? 25 & 26 August, […]

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