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Video | Korio | Anna-Zeralda Canals Hamann shares how flexible IRT design can help sponsors prepare for changes in supply strategy, dosing, and patient cohorts. Effective RTSM systems are designed to manage uncertainty without disrupting trial operations. |
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Webinar | PPD Clinical Research Business of Thermo Fisher Scientific | Explore how the new ICH E6 (R3) revisions are reshaping clinical trial oversight and examine how AI-driven tools like the Clinical Decision Suite can help sponsors enhance trial efficiency. |
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Webinar | BRANY | Learn how ethics and biosafety review boards work together to protect participants in gene therapy trials for neurological conditions, including consent and safety monitoring. |
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Video | Dr. Vince Clinical Research | Explore how clinical staffing, monitoring equipment, and structured safety oversight support the safe conduct of Human Abuse Potential studies, including approaches to adverse event management. |
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Video | IQVIA Technologies | Unlock real-time data tracking, customizable reporting, and proactive compliance monitoring with the IQVIA eCOA Sculptor Portal to enhance clinical decision-making and ensure protocol adherence. |
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Video | Clinical Leader | In this final Trials Without Borders webinar, we explore topics such as data compliance for global trials, logistics of shipping biologics to Australia, and how Australia’s regulatory speed and site collaboration make it a strategic launchpad for early-phase studies. |
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