About Cori Clinical
Give the time back to the science.
Researchers set out to advance science, then spend the week carrying each decision by hand into every document it touches. We build the trial so the decision is made once, and every document follows.
Where the time goes
Vision
No patient waits for science that's ready.
Mission
One platform for the entire trial startup, so the science never waits on the process.
Why we are building it
Clinical development deserves better.
Cori is the system behind better clinical trials. It takes on the regulatory and administrative work around a trial: authoring, reconciliation, impact mapping, submission assembly.
Human expertise stays in charge. Cori authors and flags; your team approves. Nothing reaches a document without someone putting their name to it.
We are building the best-in-class AI system for clinical trials.
Jorn & Patricio
Co-founders of Cori Clinical
Investors and advisors
Maarten Alblas
Founder, DataSnipper
Ben Peters
Founder, Five AI and Cogna
An Van Es-Johansson
Chief Medical Officer, Sobi
Tim Shi
Founder, Cresta and Early Research, OpenAI
Stan Boland
Founder, Icera and FiveAI
Leadership
The people you will work with.
Co-founder & CEO
Jorn Jansen Schoonhoven
Co-founder & CTO
Patricio Fernandez Weisson
Chief Clinical Officer
Emma Ogburn, PhD
FAQ
Good to know.
What is Cori, and how does it help clinical trial teams?
Cori is AI for clinical trials. It holds your study as one structured record and authors the documentation from it: protocols, informed consent forms, regulatory submissions. Cori authors and checks; your team approves. A change made once carries through every document instead of being re-typed into each one.
Which types of clinical trial documents does Cori support?
Across the documentation of trial startup, with each artefact kept consistent with the others:
- Study protocols and protocol amendments
- Investigator brochures
- Informed consent forms (ICFs)
- Case report forms (CRFs)
- Clinical study reports (CSRs)
- Common Technical Document (CTD) modules for regulatory submissions
- Site and sponsor communications
How does Cori integrate with existing workflows and systems?
Cori fits the processes you already run:
- Flexible document import and export, working with Word, PDF and regulatory submission formats
- Microsoft Word add-in, so you can edit documents directly with Cori
- Collaboration tools to assign tasks, track changes and manage approvals within your team
How does Cori help with regulatory requirements?
Cori is built to align with FDA, EMA, ICH-GCP and local requirements. It pulls the relevant guidance for each document, flags missing elements, and shows where the protocol and the participant-facing materials disagree. The judgement belongs to your regulatory team; Cori shows them what to look at. Cori Clinical holds ISO/IEC 27001 certification and complies with the GDPR and the EU AI Act. HIPAA is supported under a Business Associate Agreement, and 21 CFR Part 11 support is in progress.
Is Cori secure, and how is data protected?
Yes. The controls that back that up:
- AES-256 encryption at rest, TLS 1.2 and 1.3 in transit
- None of your data is used to train models, under a zero data retention policy
- Role-based permissions to restrict document access
- Audit logs, so every action is tracked and attributable
- Cloud infrastructure monitored continuously for threats and anomalies
How can I try Cori or request a demo?
Book a demo and we will walk through the platform on your own study, not a sample one.
Happy to go deeper on any of this.
Book thirty minutes with us.