All articles by Raavi Tangirala
Safe passage: data control in the clinical trials cold chain
Balancing risk and cost is a delicate undertaking where controlled room temperature clinical trial shipments are concerned. Lisbeth Nielsen, senior clinical supply technician at Lundbeck Pharmaceuticals, tells Andrew Putwain how proper monitoring improves safety and saves money.
Safety fast: ensuring drug safety during clinical trials
Risk-based monitoring can promote more efficient data standardisation and speed up clinical trial timelines. Kerry Taylor-Smith speaks to Hanne Cloetta Lang, vice-president at Novo Nordisk Clinical Operations, about how technology can identify critical values in studies to minimise the number of sites monitored and reduce costs.