End-to-end clinical supply optimization brings many benefits including increased transparency and efficiency as well as risk management, ensuring 100% patient service levels. But it also results in freeing up manufacturing time and being able to start new trials sooner. Learn more about how end-to-end clinical supply optimization can accelerate time to market: Also […]read more
Join us at the Clinical Trial Supply Forum, in Brussels. On May 20th, Sébastien Coppe, Head of Consulting Group at N-SIDE, will be co-presenting with Didier Basseras, Vice President Clinical Supplies at Sanofi-Aventis : “Evolving from Push to Pull Clinical Supply Chain Management with Early Phase Optimization” The participants will learn how to : Optimize […]read more
Visualize your data to manage your clinical trial at a glance and facilitate your decisions. N-SIDE is happy to launch the new Clinical Trial Management Dashboards. Our business intelligence analytics leverage all of CT-FAST clinical trial forecasts, IRT study data and project information, turning data into insights. Make informed decisions and quickly visualize your […]read more
Join Jay Dexheimer , Head of Business Development – US, at the Clinical Trial Supply Chain Strategy Meeting East Coast 2019 meeting on June 13th in Boston. Jay will lead a roundtable discussion on “Managing ROI in Forecasting Clinical Supplies” Participants will learn about: Various types of forecasting systems along with amount of information / […]read more
Maximize the supply friendliness of your clinical trial protocol – start optimizing at protocol design!
Critical decisions are taken during protocol design. It is essential to maintain patient centricity and respect site constraints, but it is also an opportunity to evaluate the supply impact. Different scenarios can be investigated with an advanced simulation and optimization tool that accurately models both the clinical design and the supply aspects of the protocol. […]read more