Effective Use of an IRT Platform for Clinical Supply Chain Management

Clinical Trials, Life Sciences, Pharma Manufacturing & Supply Chain,
  • Thursday, May 30, 2019 | 11am EDT (NA) / 4pm BST (UK) / 5pm CEST (EU-Central)
  • 60 min

The way in which clinical supplies are managed can make or break a clinical development budget. Clinical supply management decisions often result in significant overage and waste as a risk mitigation tactic against insufficient supplies and compromised trial outcomes.  Bryan Clayton and Korinne D’Orsi discuss how to optimize the balance between shipment and packaging costs using an IRT system.

  • Fixed and variable costs must be managed closely
    • While both shipment and packaging costs can be unplanned for and play a significant part on a study budget, effective use of an IRT can reduce some variable costs.
    • Reducing clinical supplies overage can save hundreds of thousands of dollars if planned correctly.  Often distribution costs can be escalated by unseen global shipments, so it is critical to appropriately manage your resupply strategy.

Attendees will learn about the historical context of IRT, the impact of increased clinical trial complexity on clinical supply management and how technology replaced randomization by packaged design. Additionally, this webinar will discuss key stakeholders, and when to get them involved.

Speakers

http://Bryan%20Clayton,%20YPrime

Bryan Clayton, Vice President, Strategic Solutions, YPrime

As Vice President of Strategic Solutions, Bryan Clayton collaborates with biopharma executives and clinical operations and supplies teams to define, plan and implement eClinical technology. Prior to his appointment in business development leadership, Bryan spent more than five years in operational roles involving eClinical products. Most recently, he served as Manager of R&D for YPrime’s interactive response technology (IRT). Earlier, he oversaw project management and the teams responsible for IRT implementation at Cenduit. Throughout his career, Bryan has led numerous integrations between eClinical systems, third-party data sources and various device types.

Message Presenter
http://Korinne%20D’Orsi,%20YPrime

Korinne D’Orsi, Associate Director, Clinical Supplies, YPrime

Korinne D’Orsi is Associate Director of Clinical Supplies at YPrime, where she leads efforts to help biopharmaceutical companies with clinical supplies forecasting, demand planning and global distribution strategies. Korinne has more than a decade of experience with strategic supply chain planning, team leadership and process improvement initiatives. Korinne previously served as Manager of Global Clinical Supplies for PPD. There, she held responsibility for project and team oversight of clinical trials that typically involved thousands of patients and hundreds of investigator sites around the world. Prior to PPD, she was Director of Global Project Excellence for Marken, a global provider of clinical trial logistics solutions.

Message Presenter

Who Should Attend?

This webinar will appeal to senior professionals working within:

  • Clinical Trial Supply
  • IRT
  • eClinical Technologies
  • Clinical Operations
  • Outsourcing and Procurement

What You Will Learn

  • Methods to reduce overall cost of clinical trial packaging and shipping
  • Self-service tools typically found in best-in-class IRT systems for clinical supply users
  • Simple algorithms for estimating resupply levels and strategies

Xtalks Partner

YPrime

YPrime offers more than a decade of focused work with eClinical systems to expedite and improve the quality of patient management, clinical supplies, drug accountability and clinical data. Cloud-based interactive response technology (IRT) and electronic clinical outcome assessment (eCOA) platforms offer sponsors greater speed, precision and integration in clinical trial management.

Our data services and tools help sponsors bring together fragmented clinical research data into contextual information they can act on. YPrime’s technology and service offerings enable sponsors to move faster and more efficiently to their next development milestone.

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