EOM 1352: Fri 7 June 2024, 11:36

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Excel in Data Management During Clinical Trial Handoffs

Clinical trial clients often face the complex task of a contract research organisation (CRO) transition, moving critical trial functions from one CRO to a functional...
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De-Risking FIH: Integrated Strategies for Rapid Proof-of-Concept

The transition from preclinical to clinical testing is a pivotal moment in drug development. It’s also one of the most challenging development milestones, beset by u...
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Navigating Complexity in Master Protocols with Key Operational Partners

Master Protocols have the capacity for great advantages and efficiencies in drug development over traditional trial protocols but can be challenging for sponsors due...
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Measuring What Matters: Designing a Future-Fit FSP Model for Modern Drug Development

The Functional Service Provider model has grown from a tactical staffing mechanism into a strategic outsourcing framework that underpins modern clinical development....
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Mental Health Applications of Generative Artificial Intelligence

One of the newer areas in which the US Food and Drug Administration (FDA) is exploring its regulatory role is the use of artificial intelligence (AI) in digital ment...
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How Global Contact Centre Support Enhances Clinical Trial Success

Redefining Participant Support Through Global Contact Centres As clinical trials continue to expand across geographies and adopt decentralised and hybrid models, ens...
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Catalyst: 12th January 2026
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