E-Technologies STREAM

  1. 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.

  2. 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.

  3. 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.

  4. Maximize Control And Transparency On The Path To Study Go-Live 10/10/2024

    Simplify the historically complicated, black-box processes around eCOA solution deployment, content storage and visualization, and global go-live.

  5. IQVIA eCOA: Amplifying The Patient's Voice 4/19/2024

    Dive deep into the capabilities of IQVIA's eCOA with our expert Edward Bartels. He will focus on how to effortlessly create a diary, schedule site/participant assessments, and intuitively manage translations and compliance.

  6. Everything You Need To Know About Adopting eConsent Across Large Pharma Organizations 2/22/2023

    Did you know that the average cost for a delayed trial is between $600,000 and $8 million per day? Discover how electronic consent management technology is helping sponsors, CROs, and sites.

  7. 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.

  8. 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.

  9. Functional Work Streams: Operationally Preparing Your Teams For Successful TMF Inspections 7/14/2021

    Inspection readiness is all about preparation. Not just having your documents in order, but also your team. In this session, seasoned TMF expert McKenzie Knudson will share a proven approach to getting your team ready for inspections.

  10. 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.