Trusted partner to global pharmaceutical organisations delivering temperature-controlled systems for regulated facilities.

Our team brings decades of engineering expertise and regulatory understanding to complex projects across manufacturing, distribution, R&D, and quality operations.

We work with global pharmaceutical companies, CDMOs, logistics providers and health authorities, delivering GMP-compliant cold rooms, controlled chambers, and precision environmental systems that meet both international and local standards.

From new-build developments to retrofits and facility upgrades, we manage high-value, multi-stakeholder projects with a clear focus on quality, resilience, and operational readiness.

Delivering Across Western Europe – With Local Expertise

We have successfully delivered projects in:

• United Kingdom (nationwide NHS and private sector delivery)
• Ireland (including pharma clusters in Dublin, Cork and Limerick)
• Germany (supporting API and finished product manufacturers)
• The Netherlands (logistics, stability and QA testing hubs)
• France (clinical trial and vaccine storage sites)
• Spain and the Nordics (warehouse and distribution facilities)

We understand the varying regulatory expectations, cultural practices, and technical standards across Europe. Our team works with local contractors, authorities and site teams to deliver seamless cross-border projects that meet EU GMP, MHRA, and FDA requirements from design through to validation.

What We Deliver

We design, install and maintain:

• GMP cold storage facilities (+2°C to +8°C, -20°C, -80°C)
• Stability testing chambers for ICH Zones I–IVb
• Quarantine and controlled drug storage areas
• Ultra-low temperature storage for biologics and cell therapies
• Cleanroom temperature and humidity systems
• Ambient controlled warehouses (15–25°C)
• Integrated alarm, monitoring and telemetry systems
• Dual-redundant environmental systems with 24/7 failover
• Validation packages for MHRA/FDA inspection readiness

All systems are tailored to your facility’s specific compliance framework, operational processes and risk profile.

Trusted by Global Pharma Clients

Our international experience spans projects for:

• Global top-10 pharmaceutical manufacturers
• Contract development and manufacturing organisations (CDMOs)
• Logistics and third-party distribution providers (3PLs)
• Biotech and cell/gene therapy developers
• Clinical trial depots and QA laboratories
• Centralised storage facilities serving national healthcare systems

We bring the technical understanding, delivery discipline and documentation standards needed to work in highly audited and regulated global operations.

Project Capabilities

We are trusted to deliver end-to-end project services, including:

Design & Engineering

• URS development
• Detailed environmental control designs
• Equipment and materials specification
• Redundancy and BMS integration planning

Installation & Commissioning

• UK and European on-site delivery teams
• Controlled environments built to GMP-grade standards
• Refrigeration, HVAC, and electrical integration
• Cleanroom-compatible installations where required

Validation & Documentation

• DQ/IQ/OQ/PQ protocol development and execution
• Temperature/humidity mapping and calibration
• Documentation aligned to MHRA, FDA and EU GMP Annex 15
• Support for client-led or third-party validation teams

Ongoing Support

• Planned Preventative Maintenance (PPM)
• 24/7 call-out across select regions
• Performance monitoring and requalification services
• Multi-site service contracts for networked operations

Supporting Multi-Site Delivery & Global Frameworks

We support long-term partnerships with global clients, including:

• Multi-site rollout programmes across the UK and Europe
• Consistent engineering specifications and validation protocols across international sites
• Centralised documentation templates and digital delivery
• Collaboration with global procurement, validation and quality teams
• Integration with global audit schedules and compliance reviews

Whether working as a principal contractor or as part of a wider vendor team, we adapt to your organisation’s project governance model and reporting structure.

We Speak the Language of QA, Validation and Compliance

Our senior team includes engineers and compliance specialists with years of experience working directly in regulated pharma environments. We understand the expectations of qualified persons (QPs), validation leads, MHRA inspectors and international auditors, and we build systems that withstand scrutiny at the highest level.

We don’t just meet specs – we design and deliver solutions that meet the spirit and letter of Good Manufacturing Practice.

UK & Western Europe Coverage

Every international project is supported by:

• A UK-based project lead and single point of contact
• Local installation teams or trusted partners
• Site-specific RAMS and logistics planning
• Pre-install audits and installation sequencing
• Optional post-handover maintenance and monitoring packages

If you're planning a global pharmaceutical project or require a GMP-compliant installation outside the UK, our experienced team is ready to help scope, design and deliver it.