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Run your EU MDR PMCF program on one platform
PMCF is a multi-year evidence commitment, the post-market clinical follow-up component of your EU MDR post-market surveillance obligations,...
Data management for device studies, on one page
Device studies carry data management demands that lean teams rarely staff for, from IMDRF coding to PMCF study...
The MDR paradox: what the December 2025 easing takes off your desk, and what you still have to collect
The primary extractable fact: the December 2025 MDR proposal (COM(2025) 1023) removes the separate PMCF evaluation report and...
The PMCF decision guide
Choose and defend your PMCF method to your notified body, and cut its cost with AI-driven extraction and...
Accelerating Enrollment for Direct-to-Patient Observational Studies: A Case Study in Traveler’s Diarrhea
Discover how TrialScreen and Castor closed enrollment three months early on a fully virtual, direct-to-patient study (Travelers Diarrhea),...
Inside the Curavit and Lindus CRO deal
The decentralized trial hype has faded, but the direct-to-patient model has matured, and the teams running it now...
Castor Catalyst is the first to market to show industry-leading data extraction accuracy in a sponsor-audit-friendly technical approach
Castor Catalyst, Castor's AI-driven clinical data platform, reads data directly from source records and proposes each value for...
When patients enroll themselves, studies fill about six times faster
Self-selected and self-served: does patient-led digital enrollment predict downstream data completeness in real-world evidence studies?
Inside the Curavit and Lindus deal: what unified US and European trial delivery really takes
Curavit has acquired Lindus Health's CRO assets, bringing US and European trial delivery under one roof while Lindus...
Direct-to-Patient at Scale: What’s Working and What’s Next
The decentralized trial hype has faded, but the direct-to-patient model has matured, and the teams running it now...
Survey Compliance Dashboard
ePRO compliance usually lives in a spreadsheet, so a study team learns weeks late. Filter to participants below...
Targeted Source Data Verification
Verifying every field burns monitoring hours. Set a global or site-specific SDV plan in one click, and get...
Query Management
System-generated and manual queries side by side, each opening onto its audit trail, comments and field history. Answer...
FormSync Mid-Study Changes
Watch the FormSync demo: build and test a mid-study protocol amendment in a linked study, then merge it...
Monitoring: Queries and SDV
Queries and source data verification in one monitoring tab, each query with its audit trail, plus targeted SDV...
End-to-End ePRO Process
A separate ePRO vendor means a second build and a reconciliation step. Build surveys in the same study...
Does real-world evidence still need the physician? A live debate at the RWE crossroad
Anthropic's CEO says AI could cure most disease within a decade. The harder question is what happens to...
The Castor platform for medical device trials, on one page
Evaluating clinical data platforms for a device study takes weeks that lean teams rarely have, and explaining the...