Services · Scope defined around your need

We take care of the details behind your critical environment.

So your team can focus on the work that matters.

Primary service

Environmental monitoring systems

PLAN · INSTALL · CONFIGURE · MAINTAIN

Advanced, gap-free, real-time environmental monitoring for critical applications in life sciences, healthcare, logistics and industrial settings.

We monitor the parameters selected for your site, including temperature, humidity, differential pressure, liquid nitrogen levels, CO₂, O₂, oxygen depletion, airborne particles and other parameters you need.

Bright cleanroom corridor with glass partitions

Parameters and typical locations

Parameters

Temperature, relative humidity and differential pressure
Liquid nitrogen level, CO₂ and oxygen depletion
Airborne particles from 0.3 μm
Door status, relay outputs and 4–20 mA signals
Power loss
Other compatible parameters by agreement

Typical locations

GxP environments
Warehouses
Cleanrooms
Laboratories
Hospitals
Pharmacies
Blood and tissue banks
Other critical environments

System functions and integrations

Functions and scale

24/7 monitoring with configurable alerts
On-premises server or cloud-based deployment, according to your requirements
Reports that comply with 21 CFR Part 11 and EU GMP Annex 11
Gap-free monitoring even during power and network outages
Alarm notifications by email, SMS, voice call, lights and sirens
API integration
IQ/OQ protocols and GxP documentation
Audit trails and encrypted logging
Single-room or multi-site architecture

Equipment purchase or monitoring as a service

Equipment purchase: We supply monitoring equipment with complete installation, configuration and staff training.

Monitoring as a service: A complete service for a monthly fee, covering the purchase of the selected monitoring system and its components, installation, staff training, preventive maintenance, calibration, sensor replacement, equipment exchange and fault resolution. Technical support is available 24/7/365 under agreed service terms and a service level agreement (SLA).

GxP and audit support

GxP and audit support: We help customers define monitoring system requirements, review audit-trail and records functions and prepare for audits. We can represent customers during audits by prior arrangement. Available functions depend on the selected platform, devices and configured services. Regulatory suitability depends on system selection, configuration, validation and customer SOPs.

Performance assessment

Qualification and validation within GxP regulations

URS · IQ · OQ · PQ

Equipment and spaces

Refrigerators and freezers
Incubators and cold rooms
Other equipment or manufacturing processes within GxP regulations

Project scope may include

Design, Installation, Operational and Performance Qualification (DQ, IQ, OQ, PQ)
Temperature mapping and measurement data
Agreed protocols and a final report

Example 3D temperature mapping plan with eleven labelled probes, room dimensions and clearances from walls, floor, ceiling and doorway

Scope and documentation

We define the work around intended use and agreed requirements, then verify that the configured system meets them through documented, risk-based testing. Depending on the system and agreed scope, documentation may include a risk assessment, requirements-to-test traceability and IQ/OQ or performance qualification records. The final scope is aligned with your procedures and operational needs

URS, DQ, IQ, OQ and PQ explained

PROJECT ROADMAP

URS · Roadmap before design or purchasing begins

Define intended use and critical requirements before design or purchasing begins, creating a clear baseline for the project.

BEFORE INSTALLATION

DQ · Verify the design

With vendor input, verify that the proposed design meets the URS and addresses process, product, quality and regulatory requirements before installation.

AFTER INSTALLATION

IQ · Verify installation

Check installation against approved drawings and manufacturer requirements. As applicable, verify components, services, supplier documents, maintenance needs, instrument calibration and construction materials.

FUNCTIONAL TESTING

OQ · Test operation

Test that functions work as designed and confirm defined operating limits, including upper, lower or worst-case conditions where required. OQ results can inform procedures, staff training and preventive maintenance needs. IQ/OQ may be combined for some equipment.

ROUTINE CONDITIONS

PQ · Verify performance

Final stage where system performance is verified under real-world working conditions to ensure consistency and reliability. Performance Qualification (PQ) should normally follow the successful completion of IQ and OQ. However, it may in some cases be appropriate to perform it in conjunction with OQ or Process Validation.

Equipment lifecycle

Technical service

Inspect · Maintain · Repair

On-time technical support for life-science equipment—from installation and preventive maintenance to repairs and user training, delivered in line with your needs and manufacturer guidance.

Installation, maintenance, repair and training

Extend your equipment’s service life with our team — from installation through maintenance and repair:

Installation and setup in strict accordance with local and manufacturer requirements
Preventive maintenance planned in advance and performed on schedule
Troubleshooting and repair using manufacturer-supplied parts
Staff training on equipment application, operation, safety and operational maintenance

Service engineer maintaining an incubator in a cell bank laboratory with cryogenic storage

Equipment and consumables

Distribution of medical & laboratory equipment

Select · Supply · Support

Distribution of medical and laboratory equipment, accessories and consumables from leading manufacturers.

How we can assist

Identifying suitable products and accessories
Coordinating supply and delivery

For a product enquiry

Share the intended application and requirements
Tell us the delivery location and timeframe

Unbranded delivery truck driving through Baltic countryside

How a project moves forward

Four practical steps.

We make the expected work and required information clear before scheduling a site visit or supply.

01
Request
Describe the equipment, facility or monitoring need.
02
Scope
Agree work, schedule, access and deliverables.
03
Deliver
Complete the agreed service or supply.
04
Document
Receive agreed records, results or service information.

Have a specific requirement?

We can find a solution together

For monitoring enquiries, include the site, rooms or equipment, parameters and any existing system.

Make an enquiry