GMP-Compliant Installations

Turnkey Installation Services for Regulated Pharmaceutical and Life Science Environments

Built for Regulated Environments

We provide fully integrated, GMP-compliant installation services for temperature-controlled environments across the pharmaceutical, biotech, and life sciences sectors.


Our systems are engineered to meet the strictest regulatory, technical and operational standards, ensuring readiness for MHRA, FDA and EU GMP inspection from day one. We deliver end-to-end installation services – including controlled cold rooms,

cleanroom climate systems, freezer rooms, and stability chambers – all built and commissioned in accordance with Good Manufacturing Practice (GMP) guidelines.

Built for Regulated Environments

Every system we install is developed with compliance, control, and continuity in mind. Whether your facility handles drug substances, investigational products, finished goods, or temperature-sensitive biologics, our installations are designed to:


  • Maintain precise temperature and humidity parameters
  • Prevent unplanned downtime or excursions
  • Ensure audit-ready documentation and traceability
  • Support continuous monitoring, alerting and BMS integration
  • Comply with Annex 1, Annex 11, 21 CFR Part 11, and relevant GDP/GxP standards


We don’t retrofit commercial equipment into pharmaceutical applications – we engineer every solution specifically for regulated, high-dependency environments.

Scope of Our GMP-Compliant Installations

We deliver GMP-compliant installation of:


  • Pharmaceutical Cold Rooms (+2°C to +8°C, -20°C, -80°C)
  • Freezer and Ultra-Low Temperature Storage
  • Stability Testing Chambers (ICH-compliant)
  • Quarantine and Controlled Drug (CD) Storage
  • Cleanroom Temperature & Humidity Control Systems
  • R&D Facility Environmental Systems
  • API Storage & Process Cooling Zones
  • Packaging and Distribution Storage Facilities
  • Fully Integrated Monitoring & Alarm Systems


Each system is designed and validated to support pharmaceutical production, storage and distribution – with full URS/DQ/IQ/OQ documentation included.

Speak to Our Pharmaceutical Projects Team

Whether you are in early design stages or seeking a reliable partner for project execution, our technical team is ready to help.

Turnkey Project Delivery

We offer comprehensive installation services managed by our in-house engineering and validation teams. Our structured delivery process includes:


1. Project Consultation & Feasibility

  • Site surveys and user interviews
  • Compliance gap analysis
  • Environmental load assessments
  • Budgetary and technical planning


2. Design & Engineering

  • GMP-compliant layout and technical drawings
  • Component selection (refrigeration, control, alarms)
  • Redundancy and resilience modelling
  • Integration with existing infrastructure and BMS


3. Installation & Commissioning

  • Expert installation by qualified engineers
  • Site management and coordination with other trades
  • Safety, access and contamination controls
  • Pre-commissioning, calibration and handover testing


4. Validation & Documentation

  • Full IQ/OQ/PQ protocols and reports
  • Temperature mapping, alarm verification and failover testing
  • Audit support and training for SOP integration

What Makes Our Installations GMP-Compliant?

We go far beyond technical installation – our systems are fully aligned with Good Manufacturing Practice (GMP) principles from concept through to commissioning:


  • Design qualification (DQ) aligned to your URS
  • Materials and finishes selected for cleanability and regulatory suitability
  • Redundancy and risk mitigation engineered in from the start
  • Validation-ready components, with calibration certification
  • Monitoring, alarm and logging systems compliant with 21 CFR Part 11
  • Validation support and full handover documentation


We work in close collaboration with your QA and validation teams, ensuring a seamless sign-off process from project handover to audit.

Built for Your Environment

Our installations are used in:


  • GMP Manufacturing Sites
  • Contract Development & Manufacturing Organisations (CDMOs)
  • Research and Development Centres
  • Clinical Trial Supply Facilities
  • Vaccine Production Hubs
  • High-Containment Cleanrooms
  • Controlled Warehousing & Distribution Centres


Whether you're installing a new production suite, expanding warehouse capacity or

upgrading a facility for compliance, we ensure systems are fit for purpose and audit-ready.

Supporting Projects Across the UK &Western Europe

Our installation teams operate across the UK and throughout Western Europe, with

successful project delivery in countries including Ireland, Germany, the Netherlands,

France, and Spain.



We understand regional variations in regulatory interpretation, validation

expectations, and local facility design practices – and we incorporate these into

every installation to ensure compliance from the outset.

Speak to Our Pharmaceutical Projects Team

Whether you are in early design stages or seeking a reliable partner for project execution, our technical team is ready to help.