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Widespread clinical availability depends on strong human trials and approval from regulators

The underlying driver is the uneven pace at which national regulatory agencies are updating their clinical trial frameworks to reflect the operational realities of decentralized methodologies a structural gap that will require sustained harmonization effort across the ICH membership to resolve

Fatty acid composition of adipose tissue and blood in humans and its use as a biomarker of dietary intake

Stability of wake-sleep cycles requires robust degradation of the period protein

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Calcrea phosphorica