Featured writing from our team on the trends shaping enterprise transformation.
A conversation with Bill Draper and Keleni Tukia, MD MBA MPH, on what they heard at the BIO International Convention 2026 in San Diego — and why clinical trial imaging is at a genuine inflection point.
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Protocol deviations caught after a radiologist reads the scan cost time, inflate query volume, and create inspection risk. A protocol-aware pre-read QC gate changes all three — here’s how it works in practice.
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AI can reduce manual workload and accelerate reads, but in regulated research it must not obscure clinician accountability. Here’s how to build workflows where AI amplifies clinical judgment while preserving GCP and 21 CFR Part 11 compliance.
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As clinical trials become more complex and competitive, the role of medical imaging has never been more critical. If you’re experiencing any of these five red flags, it may be time to re-evaluate your imaging strategy.
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Clinical research is becoming increasingly data-intensive and operationally complex. Medical imaging is playing a growing role in evaluating treatment efficacy, monitoring safety, and supporting regulatory submissions across a wide range of therapeutic areas.
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Over the past several years, clinical imaging has evolved from a supporting trial function into a critical determinant of operational performance. In 2026, that shift is no longer emerging.
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