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Webinar

Clinical trials: Why drug availability
will be the next decade’s challenge

And how you can prepare for it

 

Date

June 14, 2022

Location

Online event

Timing

3pm - 4pm (CEST)
9am - 10am (ET)

DOWNLOAD THE KEY TAKEAWAY

The evolution towards innovative drugs, like biologics or cell & gene, is marking a turning point in the clinical trial landscape. The clinical supply chain is not a support group anymore, but an active driver of the success and speed of a clinical trial.

Bottlenecks or delays in drug supply are one of the causes of delays in trial timelines and a major factor in even considering a trial feasible. As the next 10 years will worsen this issue, pharmaceutical companies will have to ensure best-in-class drug waste management to stay competitive.

 

In this webinar, you will learn


  • What are the main trends impacting the efficiency of drug supply
  • How to identify the main causes of avoidable waste in clinical trials

  • What are the good practices to ensure faster recruitments and more feasible trials despite scarce drug availability
  • How clinical operations, IRT, CROs, CMC and other stakeholders also have a major role to play in achieving drug waste reduction

Webinar Recap

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About the speakers

Amaury Jeandrain's picture
Amaury Jeandrain Head of Business Development Engineering

Amaury Jeandrain is an expert in clinical trial supply and manufacturing optimization. He started his career in clinical supply chain working for a CMO before joining N-SIDE. In his 6 years of experience at N-SIDE, Amaury supported the optimization of hundreds of trials and programs from different indications and pharmaceutical companies, providing services ranging from risk-based optimization to clinical trial design and solving drug supply shortage problems. Amaury now leads a group of experts focusing on bringing knowledge about optimization to the industry.

ADA-O
Alexis Davin Clinical Supply Optimization Specialist

Alexis Davin is a clinical optimization specialist at N-SIDE and a volunteer at the GCSG. His experience in clinical supply expanded quickly by solving day-to-day supply challenges of biopharma companies. He is passionate about how digitalization can improve the clinical supply industry and, ultimately, impact patients’ health. Alexis is also supporting the development of new digital solutions to solve supply chain issues in clinical trials, which offers him a strategic view on industry trends and internal processes.

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