Trial Design Webinars
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Reducing The Burden Of PMC/PMR Studies For Sponsors, Sites, And Patients
8/19/2024
VP of Research Oncology, Neal Meropol, MD, shares how a pragmatic approach to postmarketing commitments and postmarketing requirements can reduce the burden of these studies for sites and patients.
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Advancing CAR T-Cell Therapies With Clinical Trial Customization
8/8/2024
Discover how to optimize your CAR T-cell therapy clinical trials with expert insights on genomics, flow cytometry, biomarkers, and clinical operations.
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Master Your Clinical Trial Budgets: A Step-By-Step Guide To Expense Planning
7/23/2024
This webinar explains how to create and manage successful budgets, uncover and avoid hidden costs, and minimize the pandemic’s financial impact.
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ICH E9(R1) Addendum On Estimands And Sensitivity Analysis
7/23/2024
Discover how the new framework will improve the way of designing and planning clinical trials and performing primary analyses and sensitivity analyses.
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Research As Care, A Patient Story
7/12/2024
Witness Kirsten's remarkable journey unfold as she navigates a pivotal moment that ultimately saved her life.
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A Patient's Life-Changing Experience With Diabetes Research
7/12/2024
Discover the inspiring journey of one man who battled diabetes and experienced a transformative shift in his life through a patient-focused clinical trial at the Elligo Clinical Research Center.
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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.
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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.
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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.
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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.