News|Webcasts|January 20, 2025
Mitigating Risk and Complexity in Cell & Gene Therapy Trials with IRT
Author(s)IQVIA
Webinar Date/Time: Tuesday, February 11th, 2025 at 11am EST|8am PST|4pm GMT|5pm CET
Advertisement
Even with record funding and important new launches in the cell and gene therapy (CGT) sector, trial and patient journey complexities remain major barriers to the success and sustainability of these treatments. Join us to discuss the importance of optimizing pre-trial and pre-screening activities, as well as reducing trial cost and risk, through the use of your interactive response technology (IRT) solution.
Join us to discuss strategies for mitigating the complexities of cell and gene therapy (CGT) trials while reducing risk and cost. CGTs promise critical and transformative benefits to patients. Even with record funding and new launches in this sector, trial and patient journey complexities pose significant barriers to the success and sustainability of these treatments. CGT pioneers require supply chain partnerships that mitigate trial risk and complexity and provide a consultative approach to protocol execution. This webinar will explore how to succeed by optimizing pre-trial and pre-screening activities, as well as reducing trial cost and risk with your interactive response technology (IRT) solution.
Three key take-aways
Three key take-aways
- Learn how to leverage your technology provider as a key consultant in technology and process support for protocol execution.
- Learn about ways to optimize pre-trial and pre-screening activities through flexibility and strict control of process in IRT.
- Understand how to reduce cost and risk with advanced drug supply technology.
Speaker:
Cara Woodruff
Director, Product Management, IQVIA IRT
IQVIA
Director, Product Management, IQVIA IRT
IQVIA
Cara Woodruff is a highly motivated IT product management professional with over 29 years of experience in the biopharmaceutical service industry. She executes product strategy, defines product vision and roadmaps, develops customer-driven product requirements incorporating human-centered design, drives product release cycles using Agile methodologies, and collaborates with cross-functional teams to deliver high-quality solutions on time. Woodruff’s prior roles include IT product owner, IT business partner, integrated processes and technologies POC project/product manager, predictive analytics lead SAS developer, biostatistics senior SAS statistical programmer, statistical programming manager, clinical data programmer, and associate biostatistician.
Register Free:
Articles in this issue
Newsletter
Stay current in clinical research with Applied Clinical Trials, providing expert insights, regulatory updates, and practical strategies for successful clinical trial design and execution.
Advertisement
Related Articles
- The Impact of ICH E6(R3) on Biospecimen Management
June 25th 2025
- The Top 5 Myths About eCOAs In 2025
March 25th 2025
Advertisement
Advertisement
Trending on Applied Clinical Trials Online
1
ACT Brief Episode 7: Veeva and Merck Trial Efficiency, DCT Barriers, and Glucose Monitoring Strategies
2
Summit Therapeutics’ Bispecific Antibody Shows Positive Survival Trend in Non-Small Cell Lung Cancer
3
Beyond the Algorithm: How Human-Centered AI Design Can Drive Clinical Trial Success
4
How Sponsors Can Modernize Tools to Support Physicians
5