The Importance of Fueling Your Clinical Supply Chain

Clinical Trials, Life Sciences, Pharma Manufacturing and Supply Chain, Pharmaceutical,
  • Tuesday, October 02, 2018 | 11am EDT (NA) / 4pm BST (UK) / 5pm CEST (EU-Central)
  • 60 min

The availability of medication often determines the success of an interactive response technology (IRT) solution, with stock out situations creating significant financial and operational pain for clinical teams. Using case studies, this webinar examines how mid-study supply forecasting and optimization methods were used in combination with IRT to correct the course of a study with drug availability and expiry issues.

In this webinar, you will learn more about:

  • The impact of insufficient drug to treat a subject
  • Traditional methods to optimize available supplies and project demand to mitigate risks
  • Contemporary unified IRT and Trial Supply Optimization (TSO) solutions

Speaker

Ehsan Ramezani, Senior Director, RTSM Solutions, Bioclinica

Ehsan has 20 years’ experience in the RTSM domain. He has overseen the implementation of RTSM solutions for 700+ studies and has also held roles in product and commercial strategy.

Message Presenter

Who Should Attend?

  • Clinical supply managers
  • RTSM leads
  • IRT leads
  • Clinical trial leads
  • Clinical operations
  • Clinical outsourcing
  • Clinical technology
  • Data management

What You Will Learn

In this webinar, you will learn more about:

  • The impact of insufficient drug to treat a subject
  • Traditional methods to optimize available supplies and project demand to mitigate risks
  • Contemporary unified IRT and Trial Supply Optimization (TSO) solutions

Xtalks Partner

Bioclinica

Bioclinica is a global life sciences solution provider that utilizes science and technology to bring clarity to clinical trials – helping companies to develop new life-improving therapies more efficiently and safely. Successful clinical trials require the ability to see key details and uncover hidden insights, and Bioclinica’s hundreds of experienced scientific, medical, and domain experts bring unmatched insight across the development lifecycle, from the initial protocol to post-approval. The company’s cloud-based offerings include medical imaging; cardiac safety; clinical adjudication; randomization and trial supply management and optimization; electronic and eSource data capture; site payments and forecasting; pharmacovigilance; trial management; and risk-based monitoring solutions. A true multifaceted partner to trial sponsors and Contract Research Organizations (CROs), Bioclinica offers an integrated App xChange partner ecosystem, a global network of research sites, patient recruitment services, and post-approval research expertise to provide committed, detail-focused service through all stages of drug development. The company’s thousands of employees serve more than 400 pharmaceutical, biotechnology and device organizations – including all of the top 20 biopharmaceutical companies and leading CROs – through a network of offices in the U.S., Europe, and Asia.

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