Rethinking Reconciliation – Smarter IRT Strategies for Faster, Cleaner Trials

Leveraging reconciliation to streamline processes, improve visibility and reduce costs. Insights into best practice & design decisions that will minimize the time, effort and cost of performing reconciliations between clinical trial systems and sites.

21

May

  • 3 PM London / 11 AM New York
  • Free
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Why attend?

Learning Objectives of this webinar:

  • Strategies for reducing the burden of reconciliation.
  • How source data affects our decisions.
  • Digital drug reconciliation and it’s benefits.
  • Clinical systems integration planning.

 

In today’s fast-moving clinical research environment, your IRT system should accelerate your study—not slow it down. Join us for an engaging session where we’ll explore modern approaches to reconciliation that reduce effort, enhance data visibility, and lower costs.

We’ll challenge outdated habits and assumptions about IRT and EDC integration and show how evolving system functionality can dramatically reduce (or even eliminate) the need for manual reconciliation—between systems, and between systems and paper.

Through real-world examples and practical insights, you’ll learn:

  • How to rethink source data in a digital environment
  • The impact and benefits of digital drug accountability
  • Why dispensation vs. assignment dates matter – and how to manage them
  • How to get more value from IRT–EDC integrations
  • Key design strategies to simplify workflows and avoid downstream reconciliation headaches

 

Whether you’re a sponsor, CRO, or site operations lead, this webinar will give you actionable strategies to streamline your trial operations and make reconciliation a non-issue.

Speakers

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Richard Coxon
IRT Project Manager, Sharp

Within Sharp IRT Services, Richard is responsible for managing a variety of different initiatives in addition to the delivery and maintenance of Client IRT systems. These initiatives include designing and oversight of new system functionality such as the Sharp Drug Accountability Modules and Shipment Management functionality. Richard also is an integral part of the development of new processes and setting best practices within the IRT department. Richard manages the team’s day to day activities to deliver multiple projects in an efficient fashion. Richard has over 8 years’ experience in clinical systems development and 11 years of clinical trial experience.

Richard trained at the University of Nottingham Medical School where he gained his degree in biomedical sciences.

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