E-Technologies STREAM
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Building One Home for Sites
7/23/2024
Watch this presentation and demonstration of One Home for Sites for the latest updates on how the industry is coming together — even competitors — to alleviate the technology burden on research sites.
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End-To-End Clinical Data Flow
6/24/2024
Explore the interconnected data flow across Veeva Vault EDC, Veeva CDB, Veeva RTSM, and Veeva ePRO to visualize how these products work together seamlessly.
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Seamless And Integrated Onboarding For Trial Participants
10/23/2024
Streamline your patient experience with a comprehensive, all-in-one solution that allows you to recruit, screen, and enroll participants remotely from the comfort of their own homes.
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An AI Action Plan For The TMF Professional
6/12/2024
Explore AI's impact on TMF processes in this on-demand webinar. Gain clarity on AI's potential, key evaluation criteria, and practical applications for enhancing TMF health and inspection-readiness.
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Industry-First eTMF AI: PhlexTMF v21
4/6/2023
Pre-trained on millions of documents and embedding the cumulative guidance of Phlexglobal’s TMF experts, uncover how teams can ensure clinical documents are “right-first-time” at document upload.
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Do You Know Your TMF Health Score?
3/31/2022
For inspection-readiness, the critical attributes of TMF health are completeness, timeliness, and quality. View our experts explore what your TMF Health Score could be and how this can be used to achieve and maintain ongoing TMF health and inspection readiness.
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Agile eConsent: Taking A Flexible Approach To Global Implementation
6/28/2022
Hear from industry experts on how they successfully combined agile eConsent technology with global regulatory expertise to increase enrollment rates and reduce both site and patient burden.
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Align eDiary Design With Assessment Schedules
4/2/2025
Ensure alignment with your study protocol by leveraging the Sculptor portal to simulate eDiary completion and top-down scheduling, allowing for real-time preview and modifications.
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Electronic Data Capture Solutions For Your Phase I and Phase IV Studies
3/12/2025
Take a cost-effective approach to meet your study's data capture, management, and analysis needs with a solution customized to your clinical trial.
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Deploy eConsent Around The World With Confidence
8/16/2022
Explore an easy, secure way to deliver highly engaging, regulatory-compliant electronic consent for trials of all types with IQVIA Complete Consent.