XiltriX
CRO laboratory with monitored freezers and lab equipment
CRO & CMO

Operational resilience for every study, under continuous GxP watch.

CROs and CMOs manage samples through six critical stages, from setup to archiving. XiltriX maps the whole journey, watching your labs, stability chambers, LN₂ tanks, and cold chain logistics, escalating deviations before they compromise a study.

Built for GxP

Protecting your study, from first sample to final report.

A CRO or CMO depends on validated, controlled conditions from study setup to long-term archiving. The sector card below maps the operational journey in six stages: the key processes, the rooms, the equipment that must stay within range, the environmental parameters to watch, the standards that apply, and where XiltriX adds value. It is the same map our engineers use when designing a monitoring system for a GxP-regulated facility.

The lab journey

Six stages, one monitoring map.

Select a stage to see the processes, locations, equipment, parameters, standards and XiltriX value for that stage.

GxP | GLP | GCP

Study setup

Key processes

  • Study & protocol setup
  • Facility qualification
  • Method validation
  • Supplier approval

Locations

  • R&D labs
  • Process development
  • Analytical laboratories
  • Stability chambers

Assets to monitor

  • Cleanrooms (T/RH/particles)
  • Lab & process equipment
  • Incubators (CO₂/O₂)
  • HVAC & utility systems

Environmental parameters

  • Temperature
  • Humidity
  • Differential pressure
  • Particles (non-viable & viable)

Compliance & standards

  • GMP | GLP | GCP
  • Qualification (DQ/IQ/OQ)
  • Calibration & validation
  • Data integrity (ALCOA+)

XiltriX value

  • Fast, validated deployment
  • Supports method validation
  • Audit-ready documentation
  • Scales to global networks
Beyond monitoring

Beyond monitoring.

The monitoring system is only part of the answer. XiltriX adds the IT and validation expertise that regulated CROs and CMOs need.

IT expertise

SSO with Active Directory, ISO 27001, full encryption, and a REST API that connects to LIMS, BMS and EMS.

Consultancy and validation

Risk inventory, URS and validation support (IQ/OQ), from design to inspection.

Visualisation, built in

Zoomable floor plans and live dashboards on any device, with wall screens built into your lab.

XiltriX monitoring dashboards shown on a laptop, tablet and phone
XiltriX monitoring dashboards shown on a laptop, tablet and phone
Proven

Proven where studies are on the line.

Proven since 1987

No customer has lost irreplaceable material because our monitoring failed.

24/7 technical support

The monitoring chain is watched around the clock. Alarms escalate to your own on-call team.

Built for GxP

GMP, GLP, GCP and GDP: validated monitoring, data integrity and audit-ready.

XiltriX detects, alerts and escalates through your own configured on-call contacts. Your team responds to alarms; the XiltriX 24/7 team keeps the monitoring system itself healthy.

Take the sector card with you.

The printable card summarises the six stages, the parameters and the standards on one page. Share it with your quality team or bring it to your next project review.

Download the CRO & CMO sector card (PDF)
FAQ

CRO & CMO: GxP monitoring for every study

What are the most critical parameters to monitor in a GxP laboratory?

Temperature is critical across all stages, from +37°C in incubators to -196°C in LN₂ tanks. Other key parameters include humidity, CO₂/O₂ for cell-based work, differential pressure and particles for cleanrooms, and LN₂ level/pressure for cryostorage. Door and power status are vital for asset security.

Which GxP standards apply to CRO and CMO monitoring?

CROs and CMOs operate under a range of GxP standards: GMP for manufacturing and processing, GLP for non-clinical studies, GCP for clinical trials, and GDP for distribution. A monitoring system must support these with validated sensors, data integrity (ALCOA+), audit trails, and qualification documentation (IQ/OQ).

How does monitoring support long-term stability studies?

Stability studies require uninterrupted, documented environmental control for months or years. Continuous monitoring of temperature and humidity in stability chambers provides a complete, audit-ready record. Any deviation is immediately flagged, with alarms escalated to the right personnel, protecting the integrity of long-term study data.

Does XiltriX respond to alarms in our labs or storage facilities?

No. XiltriX detects, alerts and escalates through your own configured on-call contacts, and your team decides who responds. The XiltriX 24/7 team is available when the monitoring system itself has a technical issue.

A practical next step

Ready to protect your studies from setup to archive?

Tell us about your facility and the studies you can't afford to compromise. We will map the GxP monitoring points with you.

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