Safety Monitoring: What Does ePRO Have To Do With It?

By Kyle Hogan

Safety monitoring – the reporting, tracking and adjudication of potential adverse events (AEs) – is vitally important to all clinical trials. Studies rely on formal safety monitoring workflows, with well-established tools for supporting them.

But what if there were other ways to achieve faster, more accurate reporting? And what role could ePRO play in making that happen?

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