07.22.26 -- Inside Protocol Scaling, Trial Auditing & Regulatory-Grade Data

Learn how we helped a company build an ecosystem to accommodate the SAP integration and a new participant workflow.

While both trial auditing and trial monitoring have the same goal of protecting participant safety and rights, they are two separate yet important pieces of the clinical trial process.

Accurate subjective ratings are central to Human Abuse Potential studies. Learn how Visual Analog Scales are administered, what influences responses, and why data collection practices are essential.

In this presentation, CRIO founder and co-CEO Raymond Nomizu delves into how sponsors can leverage the electronic source trend among sites through the use of Central eSource.

Lois Kelly explains how smaller biopharma companies can make an FSP model work even with limited budgets. She details how she built her own RFPs, compared boutique and large CROs, and emphasized governance, alignment, and relationships over cost alone.

AI is speeding clinical trials — but silos and complexity persist. Discover how connected systems and automation can enable faster, more adaptive development.