Site Preliminaries & Mobilization
Site setup, access planning, resource allocation, execution schedules and temporary requirements established before installation begins.
Construction & Installation
Turning approved engineering into coordinated facility installation.
We coordinate pharmaceutical facility installation around approved engineering, site conditions, vendor requirements and system interfaces. Each workfront is sequenced, inspected and documented to maintain design intent and prepare installed systems for commissioning, qualification and handover.
FACILITY INSTALLATIONFrom approved design to system completion
Every system, coordinated on site
Site Integration
The approach
One coordinated plan from site readiness to completion.
Installation activities are managed through a connected site sequence, with each workfront planned around access, dependencies and readiness for the next stage.
Technical interfaces, vendor requirements and site constraints are reviewed throughout execution, helping resolve issues before they affect testing, completion or handover.
Interfaces resolved earlyConnections, responsibilities and dependencies are clarified before related workfronts progress.
Readiness drives progressEach activity proceeds when the required access, information and preceding work are in place.
Build Stages
A structured sequence from site mobilisation to acceptance testing.
Keeping installation coordinated, documented and ready for handover.
Site Inspection & Reports
Site dimensions, existing conditions, interfaces and access constraints reviewed and documented to support installation planning and timely decisions.
Execution & Installation
Installation activities coordinated against approved drawings, workfront readiness, system interfaces, vendor requirements and site conditions.
Documentation
Installation records, inspection reports, approved field changes, redline drawings and vendor information maintained for traceability and handover.
Site Acceptance Testing
Site acceptance activities, where applicable, verify installed equipment and systems against approved requirements and specifications before further commissioning or qualification activities.
Systems coordinated on site
Every system, coordinated on site.
Each installation package is coordinated against approved engineering, site conditions and system interfaces to reduce conflicts, maintain sequencing and prepare the facility for testing, commissioning and handover.
Cleanroom systems and controlled-area components
HVAC and environmental-control systems
Clean and black utility systems
Mechanical equipment and piping networks
Electrical and lighting systems
Automation, ELV, BMS and EMS infrastructure
Process and laboratory equipment interfaces
Vendor-package and service connections
Frequently asked questions
What clients need to know before installation begins.
Ready for CQV Handover
We coordinate site mobilisation, site verification, installation, inspections, documentation and Site Acceptance Testing support where applicable. Depending on your project scope, this may cover cleanrooms, HVAC, utilities, piping, electrical, automation and equipment interfaces.
The timeline depends on facility size, site readiness, system complexity, material availability, vendor schedules and whether execution is phased. We develop the installation programme around approved engineering, access conditions, package interfaces and testing requirements.
Yes. We can plan brownfield work through controlled work zones, phased installation, planned shutdowns and managed tie-ins. The execution strategy considers ongoing operations, personnel movement, contamination risks and site-access limitations.
We check site execution against approved drawings, specifications and installation requirements. Where site conditions require a change, we coordinate technical review and approval, with revisions documented for traceability and final as-built records. Changes that may affect GMP or the qualified state should also be formally assessed through the appropriate change-control process.
We sequence packages around shared work areas, access requirements, system dependencies and service interfaces. Vendor responsibilities and upcoming activities are reviewed through coordination and look-ahead planning to reduce clashes between installation, access and testing.
We assess readiness against completed installation, required inspections, documentation and outstanding punch-list items. SAT is performed where applicable, while qualification progresses against approved protocols, acceptance criteria and the project’s CQV strategy. EU GMP Annex 15 recognises SAT as applicable depending on the equipment/project and requires defined acceptance criteria and authorised progression between qualification stages.
Next step in facility readiness
Installed systems must perform as intended.
As installation, inspections, documentation and site-acceptance activities are completed, systems progress into commissioning, qualification and validation to demonstrate readiness for intended operation.
