Blog tagged as Clinical Trial Imaging Compliance

Imaging as Infrastructure: Why Sponsors Must Rethink Oversight in Modern Trials
At DPHARM, Paul McCracken, Founder and Principal of RadiaNova Consulting, sheds light on the hidden challenges of clinical trial imaging and how radiopharmaceutical studies are transforming its role.
Lori
24.10.25 02:29 PM
Redefining Imaging Workflows in Clinical Trials
Moe Alsumidaie interviewed Jeff Sorenson, CEO of Yunu, and Steve Tolle, Chief Product & Technology Officer at Ignitedata, on how the updated ICH E6(R3) guidance is transforming imaging in clinical trials.
Lori
24.10.25 02:20 PM
Why Correcting Trial Imaging Errors at Central Review Is Too Late—and Too Expensive
Site-level imaging errors affect up to 50% of oncology trial reads, delaying trials and potentially censoring patients. When quality is enforced at the point of capture, error rates drop by more than 80%, saving millions of dollars and months in trial timelines.
Lori
01.10.25 12:44 PM
ICH E6(R3) Raises the Bar on Imaging in Clinical Trials—Are You Ready?
Moe Alsumidaie’s latest article explores how the updated ICH E6(R3) guidance raises the bar for imaging in clinical trials. With imaging as the primary endpoint in most oncology studies, sites and sponsors must now meet the same Good Clinical Practice (GCP) standards as other critical data types.
Lori
03.09.25 06:08 PM

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