Featured Webinars

  1. The Cutting Edge Of Pharma: AI And RWD 1/19/2024

    Taken from a spotlight session at the CNS Summit, gain insights from thought leaders from Norstella and Citeline regarding artificial intelligence and real-world data.

  2. Unlock Clinical Trial Enrollment ROI 11/3/2023

    Consider this diverse range of real-world perspectives, complemented by data-driven insights, when looking to enhance the speed, accessibility, and efficiency of clinical trial processes.

  3. Transforming Patient Engagement And Trial Experience 3/23/2023

    Listen in as industry leaders discuss how to meet the needs of multiple stakeholders while ensuring operational efficiency, study success, and enterprise scale.

  4. The Impact Of Compensation On Clinical Trial Participation 8/15/2022

    See the results of a joint survey with 1nHealth on how compensation is likely to impact participation in clinical trials, followed by a thought-provoking roundtable on this timely topic. 
     

  5. 30th Annual Pharma R&D Annual Review — Navigating The Landscape 6/13/2022

    In this webinar, discover the trends shaping pharma’s R&D pipeline, with data broken down by therapeutic area, disease, mechanism and target, and drug type.

  6. Beyond First Impressions: CTIS Lessons Learned In First 3 Months 5/19/2022

    Now that the EU’s Clinical Trials Information System (CTIS) is up and running, disclosure and transparency experts from Sarepta, Boehringer Ingelheim, Bayer and Merck KgaA discuss the ins and outs of registering clinical trials and submitting study information to the portal.

  7. CTIS Master Series 2: Preparing Content For CTIS & The EU CTR 4/18/2022

    Disclosure experts Thomas Wicks and Francine Lane explain the importance of consistency and creating a disclosure template, plain language summaries source documents, and authoring with redaction in mind.

  8. CTIS Master Series 1: Are You Ready For CTIS? 3/22/2022

    In this informative webinar, clinical trial disclosure experts Francine Lane and Thomas Wicks provide a high-level overview of EU CTR/CTIS regulations, show how they differ from the EU CTD directive, share timelines for compliance, and discuss the scope of data sharing.

  9. Leveraging AI And Machine Learning To Deliver Next Generation Feasibility & Site Selection 3/15/2022

    In this presentation delivered at SCOPE 2022, hear how ICON leveraged Study Feasibility to its advantage.

  10. Webinar: Improving Diversity In Clinical Trials 2/15/2022

    Because there are no regulations mandating study diversity, it is up to sponsors to take the lead. In this webinar, panelists discuss how trust, accessibility and technology combine to improve the diversity of clinical trial of participants.