On-Demand Webinars

  1. Reducing Macroeconomic Pressures On Clinical Trial Supply: Session 2 4/28/2023

    Join IRT industry veteran and drug supply expert Stefan Dürr for a discussion about how to reduce the impact of both traditional and emerging macroeconomic pressures on clinical trial supply.

  2. Key Considerations When Developing Your Combination Product 2/20/2024

    Succeed in combination product development by understanding the risk factors that may arise and implementing mitigation strategies that will streamline the device development process.

  3. Improving Supply Chain: Accountability, Sustainability, Optimization

    Watch as industry experts explore the advancements in drug accountability facilitated through IRT, encompassing innovative methods for managing site variations and sustainable supply chains.

  4. Addressing DtP Clinical Supply Challenges Through Speed And Flexibility 1/20/2022

    Join Neta Bendelac from 4G Clinical and Limor Teomim from IMP CSS for an informative webinar as they explore how to mitigate the growing challenges faced as a result of the pandemic when it comes to DtP strategies and virtual trial design.

  5. Agile IRT/RTSM - Enabling Clinical Trial Design And Supply Innovation 1/20/2022

    This webinar demystifies the term “agile,” from an operational perspective, while highlighting the speed and flexibility these systems offer to be able to support complex protocols that require accelerated changes.

  6. Impacting Sustainability Through Vendor Collaboration, Procurement 9/12/2024

    Guido D’Agostino, Head of Global Procurement at Chiesi, and Stefan Dürr, Senior Director of Product Management and Client Delivery at IQVIA IRT, delve into their achievements in sustainability.

  7. Navigating Regulatory Direct-To-Patient Considerations 5/20/2022

    This webinar aims to introduce the main regulatory themes, as well as provide a practical insight into converting regulatory theory to practical steps to enable DtP on global studies. 

  8. Essential Up-Front Planning For Your Clinical Trial

    Early planning mitigates risk by avoiding stock outs and study delays, minimizing waste with optimized inventory, and forecasting demand to facilitate robust supply planning.

  9. Integrating Early Development With Clinical Supply

    In the era of seamless development, reducing time to the clinic and getting rapid approval is key. An integrated approach can accelerate timelines, avoid communication pitfalls, and improve outcomes.

  10. The Catalyst Of Decentralized Clinical Trials: Combining Clinical And Digital 7/27/2022

    Decentralized clinical trials are made up of a multitude of elements, from in home clinical capabilities, logistics, digital platforms, and technology, to global reach and more. This webinar shares important factors to consider to build your DCT ‘molecule’ successfully.