In the evolving landscape of clinical research, regulatory compliance is non-negotiable. Historically, research sites relied on physical binders, paper logs, and manual filing systems to manage[...]
Read MoreAs clinical research transitions from paper-based methods to digital-first operations, eSource (electronic source data capture) has emerged as a key driver of efficiency, compliance, and data[...]
Read MoreLeveraging ICH GCP R3 and COSMOS CTMS for Modern Clinical OversightIn today’s evolving clinical research landscape, remote monitoring has transitioned from an optional add-on to a[...]
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