E-Technologies STREAM

  1. The Journey From File To Trial: Automating Regulatory To TMF 2/9/2021

    In this webinar, we explore the value of automation between the Trial Master File (TMF) and Regulatory solutions.  This connection can bridge the gap from the clinical trial to the regulatory filing, ensuring consistency of information while reducing duplicated data entry.

  2. 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.

  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. Bridging The Gap: EHR To EDC Integration In Clinical Trials 9/9/2025

    This distinguished panel of industry experts shares an engaging and honest discussion about the current state and future potential of EHR-to-EDC integration.

  5. Is It Worth The Effort To Switch To Veeva's EDC? 8/14/2024

    Kronos Bio discusses how their oncology biotech switched to Vault EDC for faster, more flexible builds.

  6. Overcoming TMF Management Challenges For Small And Mid-Sized Companies 2/10/2021

    Maintaining an inspection-ready Trial Master File is becoming increasingly burdensome, even for teams with significant resources. In this webinar our experts walk through a new, full-service TMF management approach implemented by smaller biopharmaceutical companies. By adopting a fixed-fee, turnkey model encompassing everything required for ongoing TMF health, these organizations are achieving high-quality TMF compliance – with far less effort.

  7. Should Sponsors Provide Source Document Templates? 12/9/2025

    Here, we debate sponsor-provided source document templates, weighing regulatory guidance, compliance risks, and operational impacts for smarter clinical trial documentation decisions.

  8. 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.

  9. Customer Testimonial – From CRA To Management 6/26/2024

    Join Brittany Erlandson, Sr. Manager of Clinical Operations at QuidelOrtho, as she shares her journey from CRA to management and the crucial role of Medidata's EDC system in enhancing efficiency.

  10. On-site ePRO Solutions For Flexible Data Collection Across Devices 3/17/2026

    Optimize flexible electronic patient-reported outcomes that allow participants to switch between site-owned devices, personal hardware, and remote completion.