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Xtalks, Online
2025-05-01
Early-phase clinical trials require precision and agility. Yet, managing protocol changes, patient cohorts and investigational product (IP) supply can quickly become a logistical challenge.
Adaptive trials require faster decision-making and seamless execution. Without the right randomization and trial supply management (RTSM), teams jeopardize both study success and patient safety.
The key to overcoming these challenges is not just automation—it is adaptability. A configurable RTSM evolves with your trial to mitigate risk, improve compliance and prevent costly supply disruptions. When integrated with an eClinical platform, RTSM enhances workflows and efficiency, ensuring trials stay on track.
This webinar explores why a flexible RTSM is essential for early-phase success—and how Medrio’s unified approach makes a difference.
Register for this webinar today to learn how a unified, configurable RTSM solution can drive early-phase trial success.
Keywords: Clinical Trials, Compliance, Clinical Research, CRO, Patient Safety, Regulatory Compliance, Logistics, IRT, Sponsors, Early-Phase Trials, Early Phase Clinical Trials, CT Logistics
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Organized by:
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Xtalks |
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Invited Speakers:
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Ian Davison, RTSM Subject Matter Expert, Medrio
Naji Hamim, RTSM Product Owner, Medrio
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Deadline for Abstracts:
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2025-05-01
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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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