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Xtalks, Online
2024-10-21
In today’s clinical research environment, decentralized clinical trials have become a necessity rather than an option. The pressures to improve trial efficiency, reach more diverse patient populations and maintain participant engagement have accelerated the shift from traditional models to more flexible and patient-centric approaches. However, successfully transitioning to decentralized clinical trials requires a set of essential capabilities that go beyond basic technology adoption.
This webinar will explore how pharmaceutical companies and clinical research organizations (CROs) can embrace these critical elements to stay competitive and meet evolving regulatory demands. Key topics will include the role of real-world data (RWD) in supporting patient recruitment, diversity action plans and trial site selection. The expert speaker will discuss how RWD not only facilitates recruitment but also helps design trials that meet US Food and Drug Administration (FDA)’s diversity guidelines, ensuring that therapies are effective across various demographics.
Additionally, the webinar will highlight the logistical challenges and solutions for decentralized models, such as mobile phlebotomy, remote monitoring and seamless integration with lab testing infrastructure. Maintaining data integrity while enabling remote participation is critical to ensuring trial success. The speaker will thus share strategies for navigating these challenges while maintaining compliance with FDA guidelines and ensuring operational efficiency.
Finally, they will examine patient engagement, a key element of successful decentralized clinical trials. Engaging participants throughout the trial — especially those in remote or underserved areas — ensures retention and adherence, both of which are vital for gathering accurate data.
Register for this webinar today to gain actionable insights and practical strategies in the rapidly evolving world of clinical research and ensure successful trial execution with decentralized clinical trials.
Keywords: Drug Development, Clinical Research, CRO, Patient Recruitment, Regulatory, Decentralized Trials, Decentralized Clinical Trials, DCT, Sites, Commercialization/HEOR/Market Access
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Organized by:
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Xtalks |
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Invited Speakers:
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Chaarles Fogelgren, Executive Director, BioPharma Services, Quest Diagnostics
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Deadline for Abstracts:
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2024-10-21
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Registration:
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Free Registration
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E-mail:
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tristan@xtalks.com
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