
In today's ACT Brief, we examine why defensible trial data depends on traceability and platform ownership, what CGT site readiness requires as therapy moves to community care, and why data harmonization is AI's primary bottleneck.
NAMSA replaced its paper-based system for managing clinical trial documents with Veeva Vault eTMF and has reported that eTMF has reduced the time spent handling files by at least one-third.
NAMSA, a global medical research organization, recently replaced its paper-based system for managing clinical trial documents with Veeva Systems’ Veeva Vault eTMF. The organization has reported that eTMF has reduced the time spent handling files by at least one-third, which the company says lowers costs and frees staff to focus on more value-add work for clients.
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