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The evidence gap in Hematology: From trial endpoints to patient outcomes
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As hematology trials become more complex, sponsors face increasing pressure to accelerate development while generating stronger evidence, mitigating recruitment risk and supporting faster patient access. Join Parexel's experts to discover how RWD/RWE can help you make smarter decisions earlier, mitigate risk and strengthen your path from development to approval. Don't miss this opportunity — register today.
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CLINICAL TRIAL TECHNOLOGY
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Your Trial Shows Up In AI. Now What?
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Guest Column | By Ross Jackson, Ross Jackson Consulting
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AI can explain your trial — but can it help patients act? Ross Jackson shares how sponsors can turn visibility into trust and next steps.
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Modernizing The Clinical Trial Patient Journey
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Article | By Kathy Kohler, Suvoda
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Experience how unifying travel, payments, and study tasks into a seamless journey reduces participant and site strain while keeping clinical trials on track.
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Your Medical Imaging Workflow Solution
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Brochure | AG Mednet
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By addressing common "pain points" such as the complex handling of DICOM files and unreliable transfer methods, the Judi platform prevents workflows from coming to a grinding halt.
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Clinical Trial Management System (CTMS) Interface
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Brochure | McCreadie Group
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With real-time updates for protocols, participant records, enrollments, and contacts, this CTMS Interface reduces manual entry, improves compliance, and minimizes data errors.
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Patient organizations are moving beyond advisory roles to become active drivers of rare disease drug development. Join Craig Lipset and Dr. Derk Arts to explore how patient-led registries, natural-history data, real-world evidence, drug repurposing, and master protocols can help derisk clinical development. Discover what this emerging model looks like today, where its limits lie, and how clinical-development leaders can learn from early pioneers. Click here to learn more.
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