AI in eCOA: What Works. What Breaks
AI is being applied to eCOA localization, but most teams are still figuring out where it genuinely helps...
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The Temporal Conundrum: Bridging the Gap Between Manual UAT and AI Automation in eCOA
Manual eCOA UAT runs 12-16 weeks because time-dependent protocol logic must be tested across a study's full duration....
Leveraging the patient voice to reduce regulatory uncertainty during submission
Learn how PRO data closes evidence gaps in FDA and EMA submissions. Join outcomes expert Ari Gnanasakthy and...
Castor Product Spotlight: New On-site ePRO
Watch this on-demand Product Spotlight to see Castor’s On-site ePRO in action. Our experts show how on-site capture...
Broken at Baseline: Why eCOA Fails in the Real World (and Why We Don’t Talk About It)
Why are baseline PROs still going uncaptured in 2025? Join Ari Gnanasakthy, Katja Rudell & Derk Arts to...
FDA’s Vision on PRO/eCOA Collection for RWE: Timing and Methods Explained
Watch back as our panel of experts discuss how the FDA views the collection of patient-reported outcomes for...
Castor Product Spotlight: What’s new in 2024?
In this on-demand webinar, we delve into the latest product updates on eCOA, data entry, reports, and dashboards....
Under Pressure: How Aktiia Brought Their Continuous BP Device to Global Markets with high quality data
Watch this on-demand LinkedIn Live webinar with Castor CEO & founder, Derk Arts, featuring fellow data-driven pioneer, Jay...
Introducing Castor Connect
Watch this webinar for tips on how to ensure research continuity during COVID-19 by running your trial with...
How to create patient surveys in Castor (ePRO/eCOA)
In this webinar, we teach how to send questionnaires / electronic patient-reported outcomes (ePRO) to patients that will...
