EOM 1352: Fri 7 June 2024, 11:36

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A New Breed of Digitisation: The Path to Congruency and Faster Study Start-up

Most clinical research institutions believe their study start-up delays are a technology problem. They aren't. It’s a fragmentation problem, and many technologies ha...
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Going Global: Assuring Supply in a Rapidly Evolving and Increasingly Volatile Clinical Trials Landscape

The globalisation of clinical research is accelerating, with a growing share of trials now conducted in emerging markets across Asia, Latin America and Africa. Ventu...
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The Mandate for Automation How AI is Transforming Adverse Event Reporting in Clinical Trials

The primary goal of drug safety, or pharmacovigilance, is the detection, assessment, understanding and prevention of adverse effects or any other drug-related proble...
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How RBQM Fits into An AI World

Risk-based quality management (RBQM) is now widely recognised as crucial to improving data quality and clinical trial efficiency. Regulatory backing and increasing c...
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Digital Medication Adherence in Clinical Research

Reliable medication intake is a fundamental prerequisite for both therapeutic success and the validity of clinical trial outcomes. Deviations from prescribed regimen...
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Patient-Centricity in Rare Disease: Accelerating the Path to Treatment

More than 300 million people worldwide live with a rare disease, representing up to 5.9% of the global population. With over 6,000 distinct conditions, 72% of which ...
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