Solutions > CTMS
Clinical Trial Management System (CTMS)
Medrio CTMS software, powered by Engility®, brings structured oversight to study planning, site management, and monitoring. Strengthen operational governance and support due diligence readiness from first-patient-in to study close.
Regulatory-Ready Operations
Demonstrate compliance with Good Clinical Practice with audit-ready information for any due diligence needs.
Real-Time Oversight
Track real-time enrollment, milestones, and quality. Identify and manage risks before they impact your timeline.
Rapid Study Deployment
Go live in weeks, not months. Our cloud-based CTMS is pre-configured for agility and ease-of-use, eliminating long setup delays.
Centralize Your Clinical Operations
Fragmented data kills productivity and increases risk. Medrio CTMS centralizes site, investigator, study, and monitoring information in one structured system of record, creating a documented operational foundation that supports audit readiness and future development programs.
Scalable Clinical Trial Software
Built for emerging biopharma, medical device & diagnostics sponsors and CROs, Medrio’s CTMS scales with you. Avoid the complexity and cost of legacy enterprise systems while gaining the features you need like automated monitoring, visit reports and milestone tracking.
Integrated Compliance Engine
Don’t just file documents, automate compliance. Medrio unifies essential eTMF capabilities with your EDC and study data, automatically filing documents and tracking missing records to maintain continuous inspection readiness without manual effort.
What Medrio Customers Are Saying
Find out why Medrio has a 98% customer retention rate.
“Built with the builder in mind.”
“One of the easiest systems to implement mid-study updates. Queries are easy to find and respond to. Audit trails are straightforward as well.”
Dan Pontoriero
“The entire team is exceptional.”
“They are reliable and meet timelines. I got the same team members from beginning to end. Working with Ramana was a breath of fresh air!”
Claudia Ramos
SR. DIRECTOR, CLINICAL OPERATIONS
“Data simplified!”
“Medrio provides a system that is versatile and simplifies the complexities of data collection and management for administrators and data managers.”
Anonymous
OUR INTEGRATED SUITE OF SOLUTIONS
Validate faster with the industry’s most trusted, no-code EDC. Get enterprise-grade data rigor without the complexity or cost.
Proudly Serving Life Science Innovators
Our commitment extends beyond providing solutions; it’s about being a part of a collective effort to drive positive change and innovation in critical sectors of the life science industry.
Frequently Asked Questions
How do I evaluate & choose the best CTMS software vendor?
The best clinical trial management system vendors prioritize agile efficiency over enterprise complexity. For small to midsize biopharma or CROs and startups, look for CTMS software that offers a model designed to deliver speed and control. Rapid implementation, guaranteed compliance, and centralized data should be balanced with high-touch expert services to bridge resource gaps.
What is the difference between a CTMS and an EDC system?
While an electronic data capture (EDC) system captures patient data, a clinical trial management system (CTMS) refers to managing operational data like enrollment, milestones, and quality metrics. Medrio’s core strength is a unified experience where EDC, ePRO, eConsent, RTSM, and CTMS integrate as one source of truth.
Why is Medrio among the leading CTMS vendors for 2026?
Medrio CTMS stands out against legacy giants like Veeva CTMS, Medidata CTMS, and Oracle CTMS by offering rapid deployment, modern agility, and total autonomy. Our platform is a top Rave CTMS alternative, purpose-built to help fast-growing CROs and medical device companies scale without the rigid complexity of older systems.
How does Medrio CTMS integrate with eSource, EDC and eTMF?
Medrio CTMS eliminates compliance gaps by automatically linking operational data to study documentation. Through a seamless CTMS and EDC integration, subject and visit data captured at the source flow directly into your unified clinical trial management system with no manual reconciliation required. By unifying Medrio EDC, Medrio CTMS, and Medrio eTMF, you create a single source of truth that automates monitoring and filing workflows, allowing for a frictionless transition between study phases.
Is Medrio among the best CTMS solutions for smaller biotech companies & CROs?
Yes, Medrio is the right-sized CTMS partner for scaling companies looking to centralize and automate their trial monitoring. With Medrio CTMS, smaller teams can maintain total operational control, strengthen governance, and feel confident in audit readiness from startup to closeout, without overpaying for unused features.
Does Medrio CTMS ensure compliance with 21 CFR Part 11 and GDPR?
Yes. Medrio CTMS addresses clinical data privacy and audit trail requirements through a foundation of industry regulatory compliance and best practices. Additionally, Medrio CTMS is protected by robust security measures, role-based access controls, and data encryption.
What is a "site-centric" CTMS and does Medrio support it?
Medrio CTMS supports a site-centric approach by reducing the data entry burden through a unified clinical trial management system. Because our CTMS is integrated with Medrio EDC, sites can capture data once at the source, eliminating double data entry that often slows down study coordinators. This focus on ease-of-use allows site users to spend less time on administrative tasks and more time on patient care.
Can Medrio CTMS automate the management of investigator payments & financial tracking?
Yes, Medrio CTMS can introduce automated processes for site payments based on milestones completed in the EDC. This provides financial transparency and eliminates the manual reconciliation errors common in spreadsheet-based tracking.
What is a typical timeline for CTMS implementation & data migration through Medrio?
While most CTMS solutions require months to go live, Medrio CTMS enables teams to launch in a matter of weeks. We provide a frictionless transition for those moving from legacy spreadsheets or systems like Oracle, preserving your historical audit trail throughout the migration.
Upholding the Highest Compliance Standards