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| Webinar: What’s Working in AI-Enabled Respiratory Trials: From Recruitment to Site Readiness | Respiratory clinical trials face growing challenges, from shrinking patient populations and complex protocols to competition for patients and sites. How can AI and digital solutions help? This webinar explores practical approaches to optimize study design, predict enrollment, reduce participant burden and detect emerging risks earlier. Discover how technology can support efficient, patient-centric trials while strengthening quality and execution. Click here to learn more. |
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Video | Korio | A must-watch for anyone optimizing clinical trial IRT workflows, this video explores why clinical supplies should be involved from day one. |
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Webinar | BRANY | Explore ethical and regulatory challenges in neurological gene therapy trials, with expert insights on IRB/IBC collaboration, consent protocols, and oversight for vulnerable populations. |
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Webinar | PPD Clinical Research Business of Thermo Fisher Scientific | Discover how new approaches can improve patient assessment, enable precision medicine, and help address key challenges in developing effective obesity therapies. |
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Video | Scout | Participants and sites need support that matches their language, local hours, and regional expectations. and Global Patient Liaison teams help to create a more human trial experience. |
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Video | Dr. Vince Clinical Research | Master the complexities of renal and hepatic trials by leveraging site expertise and PK modeling to navigate recruitment challenges and ensure precise dosing for impaired patient populations. |
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Webinar | TruTechnologies | Where does AI actually add value in drug development—and where does human expertise still matter? Explore practical answers for trial teams navigating the hype. |
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Webinar | Worldwide Flex | Struggling with slow study starts or operational strain? See how tech-enabled FSP models help trials launch faster and run more smoothly. |
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Video | CRIO | Accelerate your trial startup and reduce site burden with a central eSource that allows sponsors to develop and publish central source templates to sites. |
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Video | Clinical Leader | Elizabeth Jungman describes how early retirement programs and workforce reductions led to the loss of highly experienced FDA leaders, creating gaps in institutional knowledge that affect complex regulatory decisions. |
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