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End the surgical data entry burden: AI-assisted, human-supervised, 80% faster
On May 6, 2026, Castor and SAGES are hosting a 30-minute session on ending the surgical data entry...
Beyond the EHR: meeting the FDA’s new real-world evidence standards
The FDA’s December 2025 device guidance and March 2026 ICH M14 adoption raise the bar for RWE programs....
Better Evidence Starts with Better Infrastructure
Meet Castor at ISPOR US 2026 | May 17-20 | Philadelphia, PA
Schedule a meeting with the Castor team at ISPOR US 2026. See Castor Catalyst AI for real-world evidence...
Phase 4 and real-world evidence: not a spectrum, a strategic choice
Phase 4 is a post-approval interventional trial that fulfills regulatory commitments. Real-world evidence spans PASS, PAES, HEOR, natural...
Castor Joins C-Path eCOA Consortium, Surpassing 300 Industry Study Milestone
Castor joins the Critical Path Institute (C-Path) eCOA Consortium, bringing insights from 300+ industry studies to advance participant-centric...
ICH E6(R3) is here: what your centralized monitoring strategy needs right now
ICH E6(R3) is in effect. Castor's recap covers centralized monitoring, sponsor accountability, and closing the biotech RBQM gap.
SCOPE 2026 Meet us at Booth #1612
February 2nd – 5th | Rosen Shingle Creek in Orlando, Florida
Join Castor at SCOPE US 2026, February 2-5 at Orlando's Rosen Shingle Creek. Discover how our "self-driving" clinical...
Castor Catalyst
Castor Catalyst revolutionizes real-world evidence generation by automating data extraction from EHR and claims data. Built with AI-driven...
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...
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...
How a 3-Person Team Got to Phase 3 — Without the Overhead
Gameto proves you don’t need a large CRO or a floor of data managers to run complex global...
From Hype to Health: What Sword Health Got Right About Evidence
Sword Health didn’t follow the typical digital health playbook. Instead of rushing to market, they invested early in...
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...
From Hype to Health: How Sword Built Evidence That Scales
How Sword Health used long-term clinical validation to scale, prove outcomes, and build real credibility in digital MSK...
How the Gameto Team Built a Phase 3 Trial Engine from the Ground Up
Discover how Gameto designed a lean, data-driven trial strategy and scaled to Phase 3 using Castor to accelerate...
Real-world evidence factsheet
Download our RWE factsheet to view an overview of our services.
Unlocking FDA’s Vision for PRO Collection in RWE: Timing, Methods, and Insights
Discover FDA's guidance on collecting PROs for Real-World Evidence (RWE), focusing on timing, methods, and improving data quality.