Featured Webinars

1. Plain Language Summaries Becoming A Mandate Worldwide 6/13/2024

   A growing number of countries are requiring clinical trial protocol and results disclosures to be written in plain language, influencing how these documents are authored.

2. Navigating The Clinical Trial Diversity Maze 5/15/2024

   Gain comprehensive insights into diversity action plans in clinical trials through this informative presentation, focusing on the latest FDA guidelines for collecting race and ethnicity data.

3. Managing A Continually Evolving Disclosure Landscape 2/20/2024

   Compliance is more important than ever. Keep up with how regions are enforcing disclosure requirements by learning how to adjust compliance strategies accordingly.

4. 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.

5. 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.

6. 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.

7. 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. 
    

8. 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.

9. 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.

10. 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.