Demystifying IRT Terminology
About this webinar
“Configurable” and “customizable” are two commonly-used descriptors for interactive response technology systems that support clinical trials. Interpretations of these terms can vary widely across sponsors, providers and different user levels. Designed to provide guidance to sponsors and demystify the language of interactive response technology, this webinar discusses definitions and system functionality in the context of configurable and customizable. Discussion includes systems development life cycle (SDLC) methodologies, the impact on timelines and cost and common applications in interactive response technology system designs.
Who should attend
- Clinical Operations
- Clinical Supply
- Clinical Technology
- Data Management
- Procurement/Outsourcing
What you will learn
- Definitions and system functionality of configurable and customizable interactive response technology systems
- Systems development life cycle (SDLC) methodologies
- The impact on timelines and cost
- Common applications in interactive response technology system designs
Featured Speakers
Bryan Clayton
As Vice President, Strategic Solutions, Bryan Clayton collaborates with biopharm executives, clinical operations and supplies teams to define, plan and implement eClinical technology.
Prior to business development, Bryan spent more than five years in operational roles. Most recently, he served as Manager, R&D for YPrime’s interactive response technology (IRT). Earlier, he oversaw project management and the teams responsible for IRT implementation at Cenduit.
Bryan holds a master of science degree in music technology from Indiana University, and received a bachelor of science degree in music education from West Chester University.
Partner for this event
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.
Related webinars
More from Yprime.
Intersection of Quality and Operations — A Strategy for Clinical Quality Assurance
Optimizing eCOA and IRT – Empowering the Modern Clinical Trial
Helping to Decrease the Burden of Oncology Clinical Trials with Patient-Friendly Technologies
eCOA in Clinical Trials: Trends for Today and Tomorrow
eCOA Contingency Planning and the Role of Web Backup
Data Standards for eCOA in Clinical Trials
Expert Screen Review Instead of Mode Equivalence Testing: Who are the Experts?
Effective Use of an IRT Platform for Clinical Supply Chain Management
Beyond Integration: A Unified IRT and eCOA Platform
eCOA Translations and Cultural Adaptation: Best Practices and Efficiencies
The Future of eCOA: A Panel Discussion
eCOA Data and Regulatory Scrutiny: What You Should Know
