EOM 1352: Fri 7 June 2024, 11:36

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EMA PMS: Capitalising on Centralised Medicinal Product Data – Which Way Now for Regulatory Leaders?

By 2026, IDMP compliance will become more challenging for all pharmaceutical companies operating in the EU, due to the broader adoption of the IDMP data model. Now, ...
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The Potential for Deep Learning Technology in Clinical Trials

Deep learning technology can be very strong at identifying complex patterns within large data sets and mapping them to simple classifications like diagnosing a certa...
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More Insight from Fewer Patients: Advancing Rare Disease Trials with the Net Treatment Benefit

Rare disease clinical trials face a confluence of challenges: limited patient populations, heterogeneity in disease progression, and often a lack of established outc...
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The Rare Voice that Matters Most

Who better to shape clinical research in rare disease than those living with the conditions. Patient and public involvement in clinical research is crucial for ensur...
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Basket Trials for Rare Diseases: Where Innovation Meets Unmet Need

Rare diseases, which affect >30 million individuals in the United States (US), have historically taken a back seat to more common diseases such as cancer, diabete...
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The Critical Role of Effective Sample Management in Clinical Trials

Mislabelled vials or mishandled specimens in clinical trials can compromise data accuracy, potentially affecting patient safety and outcomes. With increasing study s...
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