VIDEOS & WEBINARS

  1. Signant StudyIQ Trial Management Suite Overview 7/16/2024

    See how our dynamic and rich reporting solutions facilitate high-quality clinical data and support efficient trial management. All reports, dashboards, and analytics come standard with our eCOA solutions.

  2. Applied AI For Enhanced Data Operations 5/13/2024

    Explore practical AI applications to enhance clinical trial operations through improved data interoperability, automation, and data surveillance.

  3. Unleashing The Power Of PROs Throughout Oncology Drug Development 3/20/2024

    If you missed Signant’s webinar about optimizing patient-reported outcomes measurement strategy throughout oncology drug development, we’ve summarized the key takeaways and provided the recording.

  4. How EDC Supports Modern Clinical Trials 2/26/2024

    In this segment from Clinical Leader's Solutions Expo: EDC Showcase, Jan Breemans, Senior Director of Global Solutions at Signant Health, presents novel applications for EDC in modern trial designs.

  5. Clinical Leader Solutions Expo: EDC Showcase 1/31/2024
  6. How Can EDC Systems Support Modern Trial Designs? 1/8/2024

    Industry experts discuss how EDC solutions address nuances in modern trial designs such as flexible assessment settings as well as assist modern working practices for study monitors and data managers.

  7. Bringing RTSM In From The Cold 11/2/2023

    Watch James Stringer's presentation from the October 2023 Clinical Leader Solutions Expo: IRT Showcase to learn how site burden can be reduced by having more consolidated platforms.

  8. Clinical Leader Solutions Expo 10/24/2023
  9. 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.

  10. Optimizing Data Quality In Pediatric Trials 8/23/2023

    Drawing from her extensive expertise, Dr. Joan Busner, the chair of ISCTM's Orphan Diseases Working Group, offers insights into the challenges associated with the design and facilitation of clinical trials for pediatric and rare diseases.