Better Evidence Starts with Better Infrastructure

Meet Castor at ISPOR US 2026 | May 17-20 | Philadelphia, PA

Purpose-built for real-world studies

What we’re showing at booth 1007

ISPOR audiences run the evidence. They design the studies, model the outcomes, and defend the submissions.
The tools they choose must match that standard. Here is what Castor brings to Philadelphia.

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Castor Catalyst AI

Castor Catalyst automates EHR data extraction for
real-world evidence studies
— pulling structured data from clinical records directly into audit-ready datasets. No manual re-entry.
No reconciliation cycles. Data that regulators and HTA bodies can use straight away.

AI-powered chart review that cuts abstraction time and reduces query volume

 

See Castor Catalyst in action

EDC built for observational research

Most electronic data capture systems
were designed for interventional trials. Castor’s EDC flexes to match the structure of observational and
non-interventional studies — PASS, natural history, external control arms — without forcing your
protocol into a rigid template.

Configured in days, not weeks. Used across 16,400+ studies worldwide

 

Discover EDC features ›

Direct-to-patient ePRO and eCOA

Patient-reported outcomes are central to RWE for rare disease, oncology, and immunology.
Castor’s ePRO and eCOA solutions
capture patient data directly through validated instruments, with no site intermediary required.
Strong for non-interventional studies where patient populations are dispersed.

Validated eCOA instruments. Multi-language. Works on any device

 

Explore ePRO and eCOA ›

Data management for submission-ready RWE

Castor’s data management team works embedded within your study from protocol finalization through
final data lock. For PASS submissions, EMA natural history packages, and HTA dossiers, your
datasets land clean, coded, and audit-ready on the first pass.

Fixed-fee packages. No intermediary layers. 11-year regulatory track record

 

See data management services ›

Five good reasons to stop by booth 1007

If any of these sound like your current situation, the Castor team in Philadelphia wants to talk.

  • You are planning a PASS, natural history study, or external control arm and need a data platform that regulators accept
  • Your EHR extraction process still relies on manual chart review and your timelines are suffering for it
  • You work in rare disease, oncology, or immunology and need patient-reported outcome capture that reaches dispersed populations
  • You want real-world data that meets EMA, FDA, and HTA body standards without a data management firm adding layers and cost
  • You want to see Castor Catalyst AI in action before committing to a vendor evaluation
.

Meet the Castor team at ISPOR US 2026

Connect with us before you arrive. Our team at booth 1007 covers RWE science,
platform capabilities, and study design from day one.

Mariah Baltezegar

RWE Subject Matter Expert
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Jess Potestivo Castor

Jess Potestivo

Director of Business Development
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Angie Martinez Castor EDC

Angie Martinez

Director of Solutions Consulting
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Ready to Automate Your RWE Strategy?

Eliminate manual overhead, guarantee compliance, and accelerate your timelines by 5x.

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