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Smart Sourcing: Patient Recruitment & Retention Showcase, a virtual event for clinical teams to explore and compare top patient recruitment and engagement partners. Expect live 15-minute demos, side-by-side comparisons, real-time Q&A, and practical insights to boost enrollment, diversity, and retention. Ideal for Clinical Ops, Site Engagement, and Vendor Management teams. Leave with a vetted shortlist of partners and actionable takeaways—without the time, cost, or travel of traditional conferences.
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Webinar | Elligo Health Research®
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This webinar will feature industry leaders from the U.S. Food and Drug Administration (FDA), Freenome, Cerner Enviza, Deep Lens, and Elligo Health Research®. The discussion will also explore potential pitfalls of healthcare data as well as solutions and strategies for overcoming them.
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Video | Clinical Leader
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This episode of Trials Without Borders features executives from Etira, a biopharma focused on oncology treatments. The panelists discuss the realities of running clinical trials in Australia, covering financial incentives, regulatory processes, cultural collaboration, patient engagement, and operational nuances. Panelists emphasize cost savings, trust-building with clinicians, low dropout rates, fast ethics reviews, and the importance of strong local teams for success abroad.
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Webinar | Citeline
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Identify key regulatory hurdles that sponsors face when integrating Artificial Intelligence (AI), as well as the impact of AI on clinical trial disclosure and transparency.
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Webinar | Catalyst Oncology
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Bridging the gap between electronic health records (EHRs) and electronic data capture (EDC) systems represents one of the most promising advancements in clinical research.
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Webinar | Cencora PharmaLex
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How can integrated development planning reduce development timelines and increase your chances of commercialization success? Industry experts reveal how this approach helps avoid common pitfalls.
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Webinar | Ideagen
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Discover how integrating an innovative document review platform streamlines workflows, boosts compliance, and cuts review times by 65% from real-world Life Sciences case studies.
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