Medrio provides a cloud‑based, no‑code platform that integrates electronic data capture, randomization and trial supply management, ePRO and eConsent into a single validated solution. The system enables sponsors and CROs to configure and launch studies in weeks, apply mid‑study amendments without downtime, and maintain real‑time, audit‑ready data across sites. Built‑in ISO 9001, GDPR and 21 CFR Part 11 compliance and 24/7 support help reduce operational costs and accelerate trial timelines.
Funding
$30M raised to dateRaised to date based on public sources. This may differ from the amount the company actually raised and is based only on what is publicly available on the internet.
QCFounders
Product
Problem
Clinical trial teams often contend with fragmented data capture systems, lengthy study setup times, and cumbersome mid-study protocol amendments that delay results and increase operational costs.
Solution
Medrio delivers a unified, no‑code platform that combines electronic data capture (EDC), randomization and trial supply management (RTSM), electronic patient‑reported outcomes (ePRO) and eConsent into a single cloud‑based solution. Users configure studies through a point‑and‑click interface, enabling go‑live in as little as two weeks versus the industry average of 68 days. The platform supports zero‑downtime mid‑study changes, applying updates within a day without interrupting data collection. Built‑in compliance with ISO 9001, GDPR, and 21 CFR Part 11 ensures audit‑ready records, while real‑time data flow provides a single source of truth for sponsors and sites. Continuous 24/7 global support guarantees rapid issue resolution, typically under ten minutes, helping teams maintain momentum and reduce reliance on internal coding expertise.
Target Audience
The primary customers are pharmaceutical sponsors and contract research organizations (CROs) that require rapid, compliant trial deployment and integrated data management across multiple sites.
Features
- No‑code study builder with drag‑and‑drop configuration for protocols, forms, and randomization schemes
- Integrated suite covering EDC, RTSM, ePRO, and eConsent on a single validated cloud platform
- Real‑time data synchronization delivering a unified view of trial data across all sites
- Zero‑downtime mid‑study amendment workflow that applies changes within 24 hours
- Full regulatory compliance (ISO 9001, GDPR, 21 CFR Part 11) with audit‑ready logs and role‑based access controls
- 24/7 global support with initial response times under 10 minutes and >75 % of tickets resolved within 24 hours
- Export tools and API endpoints for seamless data extraction and integration with downstream analytics or EHR systems
- Sandbox environment for protocol reviews and hands‑on demos without affecting live studies