Every clinical trial is distinct, with specific objectives and complexities. Similarly, choices for IRT systems can range from highly customisable platforms to more streamlined "express" solutions. In an increasingly complex clinical trial landscape, sponsors are often faced with balancing efficiency, budget constraints, and trial complexity when choosing the most appropriate Interactive Response Technology (IRT) solution.
A sponsor might choose a streamlined or simplified version of IRT system for several reasons, depending on the specific circumstances of their clinical trial. We will explore scenarios where this type of IRT system can lead to quicker trial initiation and cost savings.
See how ICON Flex Advantage Express can support you as an economical IRT solution, where little to no customisation is required. We will demo how this tool provides IRT essentials such as screening, enrolment, randomisation, dispensation, cohort management, emergency unblinding/reporting, notifications and integrations. We’ll also discuss optional services such as UAT script writing, and pack list/randomisation list generation.
Engage with our speakers and panel of experts for answers to your specific questions about IRT solutions and to learn more about how a streamlined IRT system can benefit your specific clinical trial needs.
Key takeaways:
- Gain insights into the advantages of how a streamlined IRT solution can simplify your clinical trials.
- Learn when it's ideal to opt for streamlined IRT and how it can align with your study objectives.
- See a demo of ICON’s Flex Advantage Express, an IRT solution that embodies the principles discussed during the webinar
Embarking on a successful clinical trial journey requires the right tools and strategies and selecting the ideal IRT system is a critical step. Don't miss this opportunity to discover how a streamlined solution can help to achieve your goals for accelerated study initiation, greater cost containment, and more efficient resource utilization, to ultimately support the overarching aim of bringing innovative treatments to patients sooner.
Who should attend:
IRT professionals and those involved in
- Clinical supply management
- Clinical delivery/operations
- Clinical strategy
- Project management
- Procurement
- Early phase trials
- Medical device trials
Speakers:
Vijai Prakasam
Vijai Prakasam has 17 years of experience working in clinical research, primarily with interactive response technology. He has a strong operational background with significant experience in various roles in study and core product development and testing. In his current role, Vijai leads a group of specialists with operational expertise in developing and testing clinical trials in ICON’s Flex Advantage system.
Adrienne Doyle
Adrienne Doyle has over 16 years of IRT experience in clinical research and over 23 years of project management experience, and a IRT expertise in a broad range of therapeutic areas and study management.