Lab Relations
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All-In-One
CTMS Software

Perfect for 10-200 person CROs and emerging sponsors. Easy and quick to deploy. No $500k implementation.

  • ✓ CTMS (Clinical Trial Management System)
  • ✓ Intuitive and user-friendly
  • ✓ Real-time oversight, compliance, and reporting
  • ✓ FDA, GCP and HIPAA-compliant
Regulatory grade clinical stars
LabRelations CTMS System

Why clinical teams choose LabRelations CTMS

One CTMS platform.
Better control. Fewer delays.

Plan, execute, and monitor clinical trials from study setup to close-out. Keep sites, sponsors, CROs, and data aligned in one system.

  • ✓ Centralize studies, sites, subjects, and milestones.
  • ✓ Built for teams who don't have time to waste.
  • ✓ FDA, HIPAA and GDPR compliant.
  • ✓ Scale from single studies to global portfolios.

Why should you try LabRelations CTMS?

Plan & track trials
from start to close-out

Manage studies, sites, subjects, visits, and milestones in one connected system. Track progress in real time and keep stakeholders aligned across the trial lifecycle.

  • ✓ Study and site management
  • ✓ Subject enrollment and visit tracking
  • ✓ Milestones, risks, timelines, and deliverables
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Plan & track clinical trials software screenshot

Built for teams who don't have time to waste

Save time on configuration, automate routine decisions and tasks. Trigger actions only when exceptions occur, not on every run. Standardize workflows while keeping control over critical steps. Adapt automation rules as methods, volumes, and regulations change.

  • ✓ Remove duplicate entry and manual coordination
  • ✓ Define rule-based workflows, alerts, and approvals
  • ✓ Get access to our expert team for support
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Automate your workflow with LabRelations CTMS screenshot

Compliance & Reporting

Turn raw data into reliable, reviewable reports. Ensure every action, change, and approval is fully traceable. Maintain complete audit trails without adding manual overhead. Automate reporting across instruments, systems, and workflows. Make confident decisions using consistent, validated data.

  • ✓ Live up to regulations (21 CFR Part 11, (EU) 536/2014 and more)
  • ✓ Secure strict audit trails & reporting
  • ✓ Integrate, import and export data safely
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Compliance & Reporting screenshot

Purpose-built for CROs and emerging sponsors

LabRelations CTMS is designed to be the ideal solution for 10-200 person CROs and emerging sponsors.

CROs

  • ✓ Powerful study oversight and operations
  • ✓ Standardized monitoring and CRA workflows
  • ✓ Permit management and site qualification
  • ✓ Audit-ready trails for every handover
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Sponsors

  • ✓ Live status, timelines, and risk signals
  • ✓ Portfolio reporting across programs and regions
  • ✓ Real oversight and custom dashboards
  • ✓ Inspection-ready by default
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A trusted & modern CTMS

Scales from small teams to multi-site operations.

Reliable support

Practical support from experts in clinical trial workflows.

Easy to deploy new studies

Quick setup and configuration. A support team is always available to help.

Available from anywhere

Work with the same data across sites, teams, and locations.

Secure and scalable

Built for regulated environments. Scales from single studies to global portfolios.

Fully configurable

Yet built for as little configuration as possible.

Take part in the LabRelations community

LabRelations LabOps community
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LabRelations partner network events

CTMS software built for speed and control

Clinical trials are complex. Sites, sponsors, subjects, documents, deadlines, all moving at once, often across borders. When your team relies on spreadsheets and email chains to keep up, things slip. A proper clinical trial management system eliminates that noise.

LabRelations CTMS software gives you one place to plan, run, and monitor trials from setup to close-out. Configure workflows, track enrollment, manage milestones. It works the way your team works, whether that's a single study or a global portfolio.

Cut the busywork

The biggest time drain in clinical operations isn't the science, it's the coordination. LabRelations automates the repetitive stuff: status updates, approval routing, task assignments, exception alerts. Set the rules once. The system handles the rest. That means fewer hours on admin, more hours on what actually matters.

Built-in document management makes it easy to share and track documents. Compliance happens in the background, not as a fire drill before inspection.

One system, every stakeholder

A clinical trial management system is only useful if people actually open it. LabRelations keeps things simple: clean interface and role-based views. CRAs, sponsors, site coordinators, and study managers all see what they need from the same live data. No version conflicts. No chasing updates.

Connect it to the tools you already use. EDC, ERP, BI platforms.

Bottom line

LabRelations CTMS solution gives clinical teams a modern, configurable solution that cuts timelines, reduces errors, and keeps everyone aligned. From first patient in to database lock.

Let's get you started

Book my demoFree TrialRegulatory grade clinical stars

Do you want to try
our CTMS for free?

  • • Powerful all-in-one CTMS software
  • • Over 175 features (and growing)
  • • Easy-to-use and configurable
  • • Faster research. Fewer errors.
Yes, I want a free trial account

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