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Product Spotlight The Self-Driving Study with Castor Catalyst – On Demand
Join Castor CEO Derk Arts to explore Castor Catalyst, the agentic AI platform built with Google Cloud AI....
Is Your eCOA UAT Stuck in Time?
Modern clinical trials increasingly rely on complex, time-sensitive logic within eCOA systems, such as narrow compliance windows and...
The End of the “PRO Tax”: Top 10 Commercial PROs & their cost-effective alternatives
The clinical trial industry faces a "PRO Tax"—the high costs and operational delays associated with licensing and implementing...
The Silent Saboteurs: Why Rater Drift and Site Unpreparedness Cost CNS Trials More
CNS trials fail not from technology limitations but organizational factors. Research reveals 55% of sites lack adequate eCOA...
Hospital-Based eCOA Implementation: Real Challenges in Infectious Disease Trials
Hospital-based infectious disease trials face unique eCOA implementation challenges including IT security delays, staff turnover, and patient acuity...
Implications of Assessing Overall Survival in Oncology Studies
The FDA’s August 2025 draft guidance reshapes oncology clinical trials by requiring pre-specified overall survival (OS) analysis in...
The Patient Experience Paradox: eCOA Strategy Overhaul
Discover how the EMA’s new Patient Experience Data (PED) guidance and the EU HTA Regulation are reshaping evidence...
Castor Catalyst
Castor Catalyst revolutionizes real-world evidence generation by automating data extraction from EHR and claims data. Built with AI-driven...
From Months to Hours: MMC’s 5-Hour EDC Builds
Discover how a specialized CRO delivers first-in-human device studies at speed with Castor
Castor Catalyst: Launching Self-Driving Clinical Trials with Google Cloud AI
Castor has launched Castor Catalyst, an innovative AI-powered platform developed in collaboration with Google Cloud. Built on Google's...
Better Evidence Starts with Better Infrastructure
Join Castor at ISPOR Europe 2025 | November 9–12 | Glasgow, Scotland
Castor is attending ISPOR Europe 2025 in Glasgow to showcase smarter, faster approaches to real-world evidence. Join us...
Castor Catalyst
See how Castor Catalyst automates the transformation of real-world data into submission-ready study datasets. In this on-demand demo,...
Automated Evidence Generation for Regulatory-Grade Real-World Data
Manual data abstraction can’t keep up with new FDA and EMA RWE standards. This whitepaper explains how automated...
The EMR Interoperability Dream vs. Clinical Research Reality
A Practical Guide to the 21st Century Cures Act, FHIR Data, and Bridging the Gap for Regulatory-Grade Evidence
Discover the real-world challenges of EMR interoperability in clinical research. Learn how the 21st Century Cures Act, FHIR...
From PDFs to Precision: Castor Powers Up RWE in San Diego
Join Castor at DIA’s Real-World Evidence Conference | Oct 16–17 | The Westin San Diego Bayview
Join Castor in San Diego for DIA’s Real-World Evidence Conference 2025, where we’ll be launching Castor Catalyst, our...
From Gaudí to Global Deployment: Castor Builds Smarter Trials in Barcelona
Join Castor at SCOPE Europe | Oct 14–15 | InterContinental Barcelona (Fira Center)
Castor is heading to SCOPE Europe 2025 in Barcelona to showcase how sponsors can streamline global clinical trial...
On-site ePRO in Action: A Recap of Castor’s Product Spotlight
Castor’s on-site ePRO adds in-clinic PRO capture to the ePRO/CDMS workflow you already use. Staff use a site...
ICH GCP E6(R3) Implementation: Practical Approaches and Real-World Considerations
ICH GCP E6(R3) implementation requires strategic planning beyond basic compliance. This practical guide covers realistic 12-18 month timelines,...
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