EOM 1352: Fri 7 June 2024, 11:36

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Patient-Derived Tumour Organoids for Precision Screening: Operationalising GxPLevel Quality for Translational Reliability

There is a persistent gap between preclinical promise and clinical reality in oncology drug development. Two-dimensional cell culture systems derived from animal mod...
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Optimising Clinical Trials for the Era of Self-Injectable Combination Products

Self-administered injectable drug–device combination (DDC) products are entering a phase of accelerated therapeutic innovation. Demographic change, chronic disease t...
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Next-Generation Risk-Based Monitoring: The Role of AI in Clinical Trial Oversight

Clinical trial monitoring has traditionally relied on routine on site visits and exhaustive source data verification (SDV) to ensure patients’ safety and data integr...
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From Start-up to Sustainability: The New Reality of Research Site Operations

From Episodic Challenges to Structural Conditions in Clinical Research sites remain indispensable as the operational backbone of the clinical trial ecosystem. They a...
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Artificial Intelligence and Ethical Review

As artificial intelligence (AI) becomes increasingly integrated into clinical research, Institutional Review Boards (IRBs) face new challenges in evaluating associat...
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Communication is Key to Unlocking Clinical Trial Success

The importance of clear, consistent communication between contract research organisations (CRO), sponsors and trial sites cannot be stressed enough. Effective collab...
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