On-Demand Webinars

  1. Filling The Sleep Health Gap 6/13/2024

    Given the essential role of sleep in overall quality of life and its link to various chronic conditions, accurately measuring sleep is crucial for developing patient-centric therapies and enhancing public health.

  2. Mastering Scientific Communication Plans Within Medical Affairs 2/6/2025

    Join industry leaders from Anju and 9 Labs for a presentation on the pivotal role of Strategic Communication Plans (SCP) in medical affairs.

  3. 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.

  4. Accelerating Clinical Data Review With Traceable Workflows 4/17/2025

    Discover how streamlined workflows and enhanced collaboration between data managers and medical reviewers can boost clinical trial efficiency, improve data quality, and ensure patient safety.

  5. FDA's Vision On PRO Collection For RWE 9/24/2024

    In this presentation, a distinguished panel of experts illuminates the crucial role of patient-reported outcomes (PROs) in shaping regulatory decisions and drug development strategies, particularly in light of FDA expectations.

  6. 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.

  7. Leveraging Internal And External Insights For Precision Enrollment Modeling 1/28/2025

    Discover how TA Scan’s innovative Trial Feasibility Flex tool empowers teams to integrate their own insights, driving more accurate and informed projections.

  8. Accelerating Rare Disease Drug Development With Wearable DHTs 12/8/2023

    Watch as experts from ActiGraph, Bellerophon Therapeutics, and IQVIA come together to explore the obstacles and potential breakthroughs in rare disease research.

  9. RTSM Considerations For Master Protocol Oncology Studies 1/20/2022

    This webinar discusses the types of master protocols and how configurable, modern RTSM systems enable fast and seamless mid-study changes to help you efficiently run your master protocol study.

  10. 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.