The Future Of Clinical Development
While researchers are driven to advance science and improve patient care, their time and talent are often consumed by essential but time-intensive administrative work.
Today's research environment presents key challenges:
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Valuable resources consumed by routine documentation
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Innovation delayed by process bottlenecks
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Scientific talent diverted to administrative tasks
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Complex regulations creating extra workflow challenges
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Trial efficiency impacting patient participation
Cori automates regulatory and administrative workflows in clinical development without sacrificing compliance or control.
Cori doesn't replace human expertise, it enhances it, removing obstacles while keeping you in control.
Together, we deliver a clinical trial process that works for science, not against it.
We see a future where technology helps researchers handle the routine so they can focus on research and collaboration.
Jorn & Patricio
Co-Founders of Cori Clinical
CO-FOUNDER & CEO
Jorn Jansen Schoonhoven
Co-Founder and CEO of Cori, created to bring Al efficiencies to one of healthcare's most outdated workflows: clinical development. He previously led data science teams at Amazon and IBM, where he also served as Chief of Staff for EMEA. After investing in Al startups at Octopus Ventures, he founded Cori to apply what he'd seen work across industries to the critical bottlenecks in clinical trials.
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CO-FOUNDER & CTO
Patricio Fernandez Weisson
With over 10 years of experience in Al and previously Data Science Director at Evinova (AstraZeneca), and Lead Data Scientist at Sanofi. He started Cori Clinical after seeing firsthand how much time and talent is wasted on manual, repetitive work in clinical trials; and how little of Al's potential is reaching the people who need it. Cori is his way of fixing that: practical Al tools, built for the teams that need it the most.
AI LEAD
Luis Cortes Ferre
Machine Learning Engineer with a strong background in backend development for GenAl applications, working across financial services, cybersecurity, and industrial projects.
He brings both technical depth and interdisciplinary experience to the Cori
Clinical team.
FOUNDING EngIneer
Albert Vazquez Mendez
Albert has over 12 years of experience as a full stack engineer for companies like Accenture, ABB and A.Team.
Having worked on Al for the last years, he brings hands on experience in building and deploying fully functional Al applications at scale.
Clinical project manager
Deborah Wyndham
Deborah has over 10 years of experience managing clinical trials across both global and domestic studies. She's led recruitment and delivery for Phase Il trials and worked with companies including AstraZeneca, Enterobiotix, AbbVie, LabCorp, and Novartis. With hands-on expertise from CRA to CPM, she ensures every study meets GCP standards, stays inspection-ready, and runs on
Cori is an AI-powered platform that streamlines clinical trial documentation, ensuring regulatory compliance, reducing manual effort, and improving collaboration. It helps teams create, manage, and submit key documents—including study protocols, informed consent forms, and regulatory submissions—faster and with greater accuracy.
Cori covers the full spectrum of clinical trial documentation, including:
• Study Protocols & 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 This ensures consistency and compliance across all essential documents.Cori is designed to fit seamlessly into your existing processes. It supports:
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Flexible document import/export – Works with Word, PDF, and regulatory submission formats.
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Future integrations – We are working on integrations with Veeva, Medidata, and other key trial management platforms.
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Collaboration tools – Assign tasks, track changes, and manage approvals within your team.
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Cori is built to align with FDA, EMA, ICH-GCP, and local regulatory requirements. It automatically:
Extracts relevant regulatory guidance for each document.
Flags missing compliance elements and readability issues.
Detects inconsistencies between protocol documents and patient-facing materials.
Provides audit trails and version tracking for complete transparency. We are also actively working toward full HIPAA, ISO 27001, and 21 CFR Part 11 compliance to meet the highest industry standards.
Yes, Cori is built with enterprise-grade security:
Data encryption - AES-256 encryption at rest, TLS 1.2/1.3 in transit.
None of the data is used to train models and is protected by a zero data retention policy.
Access controls - Role-based permissions to restrict document access.
Audit logs - Every action is tracked for regulatory transparency.
Secure cloud infrastructure - Hosted on compliant cloud platforms with continuous security monitoring.
Cori is live and ready to use. You can sign up today or request a demo to see how it fits into your workflow. Request a demo.