Medrio

Automated notifications for supply chain and operational issues

Automated shipment approval process for trial supplies

Fully validated platform ensuring compliance with global standards including ISO 9001, GDPR, and 21 CFR Part 11

Enables participants to consent from anywhere with multi-signer support and paper consent uploads, ensuring compliance and increased comprehension

eConsent feature allowing multiple participants to provide consent through digital signature

Ability to upload and manage paper consent documents within the digital platform

Expert guidance for protocol review as part of trial preparation

Allows participants, clinicians, and observers to conveniently and accurately report outcomes with flexible data capture options

User-friendly interface for participants to report patient-reported outcomes, enhancing data quality and study efficiency

Combines data capture and management in one solution with intuitive user interface and seamless data collection

Direct access to trial data and insights at users' fingertips

Real-time data access and management keeping data clean and reducing database lock time

Integrated platform offering truly connected data flow across entire trial reducing risks like duplicate entry and lag time

Electronic Data Capture system for comprehensive clinical data collection and management

Simple algorithm configuration using Excel syntax without requiring JavaScript or advanced coding knowledge

Intuitive, point-and-click interface to configure studies quickly without requiring coding knowledge

Ability to adapt to evolving study needs with mid-study changes in as little as a day with zero downtime

Rapid deployment capability allowing studies to go live in as little as two weeks versus industry average of 68 days

Flexible services to accelerate study timelines, improve data integrity, and support effective compliant clinical data management

Seasoned project managers, data scientists, and product experts to help shorten timelines and launch risk mitigation strategies

Advanced RTSM feature enabling configuration of randomization allocation rules

Customizable randomization and trial supply management program

Robust solution to randomize, manage, and control trial supplies with advanced features like allocation rules configuration and shipment approval automation

Round-the-clock customer support with initial responses under 10 minutes and over 75% of requests resolved within 24 hours

Unique approach balancing self-service capabilities with guided support and expert assistance

Customized demonstration sessions to showcase platform capabilities

Hands-on sandbox environments for testing and validating studies before launch

Streamlined workflow for sites enabling faster, more accurate data entry and enhanced productivity