With the forthcoming FDA requirements for Race and Ethnicity Diversity Plans, sponsors will soon have to outline diverse participant enrollment and retention strategies and goals, for all phase III studies.
Citeline's new Sitetrove Diversity Module marries rich site and investigator intelligence with US patient and investigator demographics, allowing you to better assess the patient landscape and prioritize investigators that are best positioned to support your recruitment goals.
Speak with our experts to learn more.
Contact UsThe Latest Insights on Diversity in Clinical Trials
White PaperThe Need for Better Diversity Data in Clinical Trial Benchmarking and Feasibility
As of December 2022, the FDA requires diversity action plans for clinical trials. Read our thought leadership content to understand how this change will impact your trials and the future benefits of developing your diversity action plan.
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Sitetrove Diversity Module
Enabling data-driven decision making across feasibility, planning and investigator and site selection activities
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Understand how you can access data to identify and prioritize investigators with diverse patient pools and enable the planning & execution of more equitable clinical trials
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Get a deeper understanding of how having access to key patient diversity data will allow you to fulfill FDA diversity requirements for your pivotal/phase 3 clinical trials
A week of clinical trial expert insights on key industry themes is coming to you
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Webinar
Diversity in Clinical Trials: Data, Disclosure and Due Diligence
Sept. 11, 2023
A panel of experts and thought leaders discuss diversity in clinical trials with a lens on FDA regulation, ethics and the commercial impact
Sign up nowA part of Citeline Clinical Connection Webinar Week
Sept. 11-14, 2023 | 10am EST/3pm UK
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Learn more about our latest Diversity Module offering and achieve targets laid out in your Race & Ethnicity Action Plan, on time and on budget.
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