E-Technologies STREAM

  1. 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.

  2. Qualified eSignature in Electronic Consent Systems 2/25/2026

    This on‑demand session offers a clear, practical overview of the major eSignature types used in eConsent — ranging from simple electronic signatures to fully qualified electronic signatures — and explains when each is appropriate.

  3. 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.

  4. Electronic Data Capture Solutions For Your Phase I and Phase IV Studies 3/12/2025

    Take a cost-effective approach to meet your study's data capture, management, and analysis needs with a solution customized to your clinical trial.

  5. The New Era Of Evidence Generation In Clinical Trials 6/19/2024

    Learn how top pharmaceutical companies are using novel innovations to drive greater speed, scale, and access in clinical research than ever before in this webinar hosted by Musaddiq Khan, Vice President of DCT Solutions at Medable.

  6. 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.

  7. 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.

  8. IQVIA eCOA Scribe Application 3/27/2025

    Experience seamless, secure, and flexible eCOA data collection with our application designed for diverse users, compatible with multiple devices, and equipped with offline functionality and robust authentication.

  9. 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.

  10. Sanofi Reshapes Patient Experience With Digital Technologies 10/3/2022

    Sanofi has adopted a Patient Informed Research And Development model within the organization. The goal of the model is to work with patients, patient groups, and patient communities to understand the concerns of patients and ensure those voices are heard throughout the company. The company defines this approach as engaging with patients and caregivers, hearing their concerns, and translating those insights into actions that will help develop meaningful healthcare solutions. Today, Sanofi’s development programs are 100% informed by individuals from the patient communities and 100% of Phase 2 and Phase 3 trials have a remote capability built into them. 

    In this Clinical Leader Live, two clinical executives from Sanofi join Chief Editor, Ed Miseta, to discuss the new R&D model, the company’s attempts to make its trials more patient-centric, and how digital technologies and devices are helping to create a better trial experience for patients.