E-Technologies STREAM

31. 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.

32. Auto Generate Documentation 4/2/2025

    Unlock seamless software development with IQVIA’s eCOA, which automates screenshots, validation documentation, and audit trails, ensuring real-time updates, easy exports, and full traceability.

33. Study Build And Scheduler Tools 3/27/2025

    Empower your study participants with IQVIA eCOA’s tailored user experiences, flexible event triggers for clinicians, comprehensive training resources, and 24/7 support for seamless study management.

34. 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.

35. Elevating The Site Voice 3/27/2025

    A decentralized trial can be daunting for sites, but Medidata offers solutions to help site staff, sponsors, and patients move smoothly through the clinical trial process.

36. Customer Testimonial – Keya Watkins, SVP, Oncology, Catalyst 6/26/2024

    Join Keya Watkins, SVP of Oncology at Catalyst, as she discusses the transformative impact of Rave EDC in enhancing competitiveness and sponsor engagement in oncology trials.

37. Document Processing: A New Hope 8/8/2024

    Tired of slow, error-prone document processing? Discover how top companies are boosting speed and accuracy while slashing costly rework. Watch now to learn how you can achieve TMF excellence faster.

38. Introducing A Smarter, More Cost-Effective Way To Run Clinical Trials 3/13/2025

    While early-phase trials often rely on less capable, cost-effective systems, the transition to more complex studies in later phases necessitates a more robust EDC system.

39. 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.

40. 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.