Lab Relations
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All-In-One
CTMS Software

  • ✓ CTMS (Clinical Trial Management System)
  • ✓ FDA- & HIPAA compliant
  • ✓ Flexible workflows and automations
  • ✓ Real-time oversight, compliance, and reporting
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.
  • Configure workflows and integrations without code.
  • 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, timelines, and deliverables
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Plan & track clinical trials software screenshot

Optimize your workflow with automations

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
  • Configure the platform to fit your exact requirements
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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, Clinical Trials Regulation etc.)
  • Secure strict audit trails & reporting
  • Connect instruments, ERP, and BI tools
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Compliance & Reporting screenshot

Purpose-built for CROs, sponsors, and research sites

CROs

  • One view across studies, sponsors, and sites
  • Standardized monitoring and CRA workflows
  • Centralized study docs and amendments
  • 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 of CRO and site execution
  • Inspection-ready by default
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Research sites

  • Subject and visit tracking, less coordination
  • Clear tasks, queries, and training per study
  • Delegation logs and site files always current
  • Clear overviews in a single source of truth
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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.

Get started in days, not months

Quick setup and configuration with help you every step of the way.

Available from anywhere

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

Data owned by you

Customer-owned data with controlled access and auditability.

Fully configurable

Tailor objects, views, forms, workflows, and permissions to your needs.

Take part in the LabRelations community

LabRelations LabOps community
LabRelations community sharing knowledge
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 eTMF keeps your trial master file current as you go. Every change is logged with a full audit trail that meets 21 CFR Part 11 and Clinical Trials Regulation requirements. 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. Standard integrations feed everything into one operational view.

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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