Trial Design Webinars

  1. The Real Reason Why You Should Participate In Clinical Research 7/12/2024

    Ruben, a news anchor from Laredo, Texas, provides a unique perspective as the inaugural participant in a COVID-19 vaccine trial, offering unprecedented insights into his daily experiences and motivations for joining clinical research.

  2. End-To-End Clinical Data Flow 6/24/2024

    Explore the interconnected data flow across Veeva Vault EDC, Veeva CDB, Veeva RTSM, and Veeva ePRO to visualize how these products work together seamlessly.

  3. Feasibility Strategies For Research-Naïve Sites 6/13/2024

    Feasibility is not just a science, there’s also an art to it, says Nick Palumbo, director, feasibility and study start-up, at Takeda. In this clip he talks about how difficult it is for research sites with limited experience to get on a sponsors’ radar.

  4. Does The Feasibility Process Differ For Rare Diseases? 6/13/2024

    Mimi Ermens, senior director, clinical development operations, global feasibility and start-up support, at CSL Behring answers a question from the audience about whether there is a difference in how you should approach the feasibility process when dealing with rare diseases vs. common diseases.

  5. A Data Scientist's Opinion On Clinical Trial Feasibility 6/13/2024

    How do we define success in the clinical trial feasibility process? Monica Jain, director, R&D data science, Johnson & Johnson Innovative Medicine has a data science background and chimes in with her opinion.

  6. What Data Needs To Be Shared? 6/13/2024

    Nick Palumbo of Takeda explains that with feasibility in clinical trials, it has to be a “two-way street” between the sponsor and sites. He and Mimi Ermens (CSL Behring) talk about the types of questions that need to be asked and the kinds of data that needs to be shared by each stakeholder.

  7. How To Be More Proactive With Feasibility 6/13/2024

    Monica Jain of J&J Innovative Medicine talks about how technologies, real-time monitoring, and performance-based metrics have helped improve the feasibility process and make it more proactive.

  8. Exploring The Principles Integral To Rare Disease Drug Development 6/12/2024

    This on-demand webinar offers valuable insights into successful rare disease drug development, including study design, regulatory engagement, and market access strategy.

  9. Build Your Diversity Action Plan With AI And Patient Insights 5/29/2024

    Discover how AI and patient insights can help you build a compliant Diversity Action Plan and overcome barriers to achieve diverse clinical trial enrollment.

  10. Cognitive, Pharmacodynamic Testing During FIH CNS Trials 5/22/2024

    A comprehensive review of optimal timing and methodologies for cognitive and pharmacodynamic testing during first-in-human trials on CNS-active compounds.