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|Articles|September 1, 2012

Applied Clinical Trials

  • Applied Clinical Trials-09-01-2012
  • Volume 21
  • Issue 9

Applied Clinical Trials Digital Edition - September 2012

eClinical: The Use of ePRO in Diabetes Studies CRO/Sponsor: Managing the Global Supply Chain Also in this issue: Clinical Trial Funding CRO Market Size Biosimilar Development

Articles in this issue

about 14 years ago

We Still Love Paper

about 14 years ago

Flow Cytometry

about 14 years ago

ePRO in Diabetes Studies

about 14 years ago

A New Paradigm

about 14 years ago

Act cover

about 14 years ago

Regulators Must Modify Approach

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Mistral and OpenAI produced identical overall eligibility labels across 200 synthetic patient-study assessments, with criterion-level disagreements concentrated in inclusion criteria where models switch between “Uncertain” and “Not included” when records lack sufficient evidence, so model choice should be driven by deployment architecture, control, and cost rather than assumed interchangeability.
The Human Side of Clinical Trials: Before Burden Becomes Risk, Capturing Friction in Real Time
In Episode 4 of The Human Side of Clinical Trials, host Brian S. McGowan, PhD, FACEHP, chief learning officer and co-founder of ArcheMedX, Inc., speaks with Jason Riis, PhD, CEO and chief behavioral scientist at Behavioralize, about how capturing friction closer to the moment it happens can reveal unclear instructions, technology friction, and workarounds that retrospective surveys and debriefs tend to miss.