E-Technologies STREAM

  1. 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.

  2. Vault Safety-EDC Connection 6/24/2024

    Learn how to automate the flow of Serious Adverse Event (SAE) information between data management and safety systems, enabling more timely responses by Pharmacovigilance (PV) teams.

  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. Preparing For 2022 1/19/2022

    2022 will be an important year for drug development. There are many questions around changes that came into play during the pandemic. A panel of experts look back over the year and into the future to help you prepare for the coming year.

  5. 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.

  6. Optimal eCOA For Vaccine Trials 8/23/2023

    Delve into the pivotal role that technologies like electronic Patient-Reported Outcomes (ePRO) can play in generating substantiating evidence and streamlining vaccine trial operations.

  7. 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.

  8. Smarter Trials Begin And End With Greenphire 2/10/2021

    Today’s clinical trials are more complicated and demanding than ever before. They’re often global, costly and require cumbersome travel. Greenphire is changing that. With our solutions, you can manage the entire financial lifecycle for trials conducted all over the world. Greenphire works directly with leading research institutions, sites, sponsors and CROs to simplify clinical trials and facilitate stronger, more collaborative relationships. With solutions that streamline your workflows, you can focus on providing better patient care.   

  9. The Diversity Imperative: EDC And Inclusive Clinical Trials 3/4/2024

    In this EDC Showcase, experts delve into the crucial role of EDC in fostering diversity within clinical trials. Discover adaptable solutions for a more inclusive and efficient clinical workflow.

  10. Harness The Power Of eCOA In Your Next Trial

    In this webinar, explore the importance of eCOAs, how they have evolved from the standard paper diaries, and what efficiencies you can realize from them.