E-Technologies STREAM
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                    Medable Total Consent: The Future Of Informed Consent
                        2/14/2023
                    With Total Consent, Medable is transforming the consenting process – harmonizing it into one simple-to-use platform that enables trial sponsors and CROs to completely customize eConsent. 
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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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                    Digital Versus Digitized: Common Misconceptions About eConsent
                        7/27/2022
                    In this on-demand webinar attendees will learn about the common misconceptions surrounding eConsent, as well as the benefits they can realize through a digitally-enabled approach. 
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                    Rethinking Today's ePRO Delivery For Tomorrow's Clinical Trials
                        6/24/2024
                    Willie Muehlhausen, Co-CEO and Founder of Safira Clinical Research, and Tim Davis, VP of Strategy at MyVeeva for Patients, discuss how ePRO delivery needs to change to better serve modern trials. 
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                    Real-Time Data Tracking And Compliance Monitoring
                        3/27/2025
                    Unlock real-time data tracking, customizable reporting, and proactive compliance monitoring with the IQVIA eCOA Sculptor Portal to enhance clinical decision-making and ensure protocol adherence. 
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                    Rapid Study Design With The Sculptor Portal
                        4/2/2025
                    Accelerate your eCOA assessment design to streamline UAT, mid-study updates, and protocol amendments effortlessly. 
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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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                    Combining De-Identified EHR And Claims Data
                        5/8/2025
                    Learn how EHR+ Data can improve your understanding of the patient's journey in ophthalmology, urology, and neurology clinical trials. 
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                    Innovations In IRT
                        11/2/2023
                    Review the latest innovative techniques employed by IQVIA IRT, including innovations in the design, delivery, conduct and monitoring of clinical trials. 
