On-Demand Webinars
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Reduce TMF Misfiles & Metadata Errors With Next-Gen AI-Enabled eTMF
4/17/2023
Listen in as Chief Product Officer Jim Nichols, Product Manager Jim Horstmann, and VP Solutions Consulting Aaron Grant discuss issues and solutions for trial master files.
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eConsent – The Enrollment Solution For Decentralized Trials
2/1/2022
The COVID-19 pandemic and the increased technological competence required to enroll and retain research participants has left many organizations wondering how to modernize their enrollment and consent process. Find out more about the landscape and its impact in the available webinar.
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An Introduction To One Home for Sites™
4/18/2024
This on-demand webinar provides a thorough overview of why IQVIA Technologies is building One Home for Sites, how it works, and who should participate.
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Proven Practices For ePRO Adoption
12/8/2022
Industry experts discuss how a medical device company implemented ePRO to close gaps in data accuracy, reduce context switching for staff, and enhance patient convenience.
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The Rise Of The Site: Empowering Efficient Clinical Study Execution
2/18/2025
Join the Co-CEO of CRIO, as he explores research site challenges and how site-based technologies can reduce administrative burdens, enhance efficiency, and eliminate redundant one-time-use technologies.
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A Framework For Selecting Reliable Clinical Endpoints From Real-World DHT Data
2/25/2025
Dr. Andy Liu presents a case study determining which digital measure of physical activity would be a well-defined and reliable clinical endpoint in a trial including patients with diabetes.
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Leverage DHT Data As Patient-Centric Primary Endpoints
5/23/2023
See how digital outcome measures of physical activity collected from ActiGraph technology as the primary endpoint in a pivotal cardiopulmonary trial were endorsed by the FDA, marking an important milestone.
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Exploring The Role Of Wearable Biosensors Within The DCT Ecosystem
3/28/2022
In this pre-recorded webinar, experts from the industry share real-world insights and practical guidance on how to achieve success in decentralized clinical trials.
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Examining The "Why" And "How" Of Integrating Your eTMF And CTMS
6/24/2022
As requirements for improved inspection readiness and quality risk management become more critical, discover the need to create a seamless integration and data flow between the eTMF and CTMS.
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Adopting Vault CDMS Accomplishments And Lessons Learned
8/31/2022
GSK leveraged an agile approach and modern ways of working to help shorten their EDC build times. Learn how they reduced EDC build and UAT times by 50% and had all new studies built within Vault CDMS in 18 months.