We believe the next generation of therapies will reach patients faster if the people running trials have software that actually works for them. That is why every line of ProCTTH is written to empower sites, engage subjects, and give sponsors and CROs clean, blinded data they can trust.
Clinical sites are the heart of every trial. We build tools that reduce their burden, not add to it.
Regulatory compliance and security are non-negotiable — but they should feel invisible to users.
Investigators, coordinators, monitors, and subjects each get an experience tuned to their workflow.
We use machine learning to accelerate setup and insight, with human oversight and full auditability.
Multi-language, multi-region, and multi-study — built for decentralized and hybrid trials anywhere.
Every feature is measured by one question: does it help bring safer therapies to patients faster?
Founders saw sites struggling with fragmented eSource, eCRF, and patient engagement tools.
ProCTTH prototype validated with site-centric study setup and no-code form builder.
Added telemedicine, ePRO, eDiary, and IoT integrations for decentralized workflows.
21 CFR Part 11, HIPAA, GDPR compliance; role-based blinding; sponsor/CRO adoption.
Launch of the Proctthify site network — connected, certified, and future-ready.
Our team brings together clinical research coordinators, principal investigators, data managers, software engineers, and compliance specialists. We have lived the pain of legacy EDC systems and paper source files — and we are building the platform we wished we had.
Former coordinators who shape UX
Engineers focused on speed & scale
Regulatory experts from day one
Responsible automation specialists
