E-Technologies STREAM

31. Right-Size Your eConsent Approach 11/17/2023

    Delve into the art of tailoring the eConsent experience to match your study and patients' specific needs, such as crafting eConsent documents, selecting appropriate delivery models, and more.

32. At The Crossroads Of Data: eCOA And Sensors Converging For Novel Insights 5/20/2025

    Leveraging sensors and eCOA addresses increasing clinical trial complexity and ensures a more efficient and effective study design.

33. Implementing Your eCOA For Optimal Clinical Trial Success 4/19/2024

    See how having the right tools to build intuitive and patient-friendly eCOA solutions can simplify the trial experience's inherent complexity, reduce participation burden, and drive engagement and compliance.

34. 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.

35. Casebook Amendments In Vault EDC 8/27/2021

    Making casebook changes is easy in Vault CDMS, even in active studies. Use the simple, point-and-click interface to deploy changes to specific sites and subjects. Any new forms or fields are then flagged for site personnel to populate retrospectively for existing patients.

36. 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.

37. Rave RTSM: IRT Expo 11/2/2023

    Get an inside look at this RTSM solution, a full-service and unique platform-based approach to interactive response technology.

38. Customer Testimonial – Chuck Bradley, Clinical Development & Operations Consultant 6/26/2024

    In this testimonial, a Clinical Development & Operations Consultant highlights the industry-standard Medidata platform and the significant benefits of using a consistent system across sites.

39. Crossing The TMF Compliance Gap With Inspection-Ready Access For Closed Studies 4/30/2021

    Your drug study is closed, you need inspection-ready access to the Trial Master File, but your CRO is ready to get the TMF out of their system and wants to send you a zip folder full of documents. What do you do? In this session, we explore an innovative new way to ensure your TMF stays secure while remaining accessible to audits and inspectors so you can focus on getting your drug to market and not on finding documents. 

40. What It Really Takes To Adopt eConsent Across Large Pharma 3/27/2024

    Explore the benefits of incorporating consent management technology and discover practical strategies for developing effective change management and training programs.