About
Software built for clinical research sites
We work only with clinical research sites, and that focus shapes everything we build.
Mission
Automate the operational work that slows down clinical research sites — visit scheduling, document tracking, quality control and study finances — so your team can spend more time on the research.
Where we are today
Verstora is in active product development. We’re building the platform with early design partners before opening it more broadly to research sites across the United States.
How we work
- 01
Diagnosis
We audit your operation and spot the bottlenecks.
- 02
Design
We propose automations and workflows tailored to the site.
- 03
Implementation
We build the software and connect it to how your team already works.
- 04
Support
We accompany, measure and optimize, remotely.
Compliance as a foundation
21 CFR Part 11 · HIPAA · privacy by design in every delivery.
21 CFR Part 11
Traceability and electronic signature
HIPAA compliant
Secure handling of patient data
Privacy by design
Security from the first sketch
The company
- What we do
- A software platform and automation services for clinical research sites: visit scheduling, document tracking, quality control of records, and study finance tracking.
- Who we are
- A technology vendor (B2B). We do not provide medical services and we do not bill insurance.
- How we operate
- 100% online and remote, with no storefront open to the public. The service is delivered through software and remote support, and client meetings are by video call.
- Who we serve
- Clinical research sites — private clinics and physician offices that run clinical trials — located in the United States.
Based in Miami, FL.
Let’s talk about your site
Tell us about your operation and we’ll tell you where to start.