Pharma & Life Science solutions
Complex projects delivered with control and precision.
Trusted by leading pharmaceutical companies to deliver integrated solutions from design and manufacturing to installation and ongoing service.
Every phase. Every discipline.
Pharma projects demand coordination across engineering, fabrication, installation, and documentation. The capabilities below cover each discipline, individually or as a fully integrated delivery.
Project execution
Built for complex life science projects.
Pharma and life science projects are becoming increasingly complex, placing higher demands on coordination, documentation, and execution.
A structured and integrated approach ensures fewer interfaces, better control, and reliable delivery across every phase of the project.
Full project scope
From concept to operation & service.
All aspects of a pharmaceutical project can be managed either as a complete end-to-end delivery or as selected components tailored to your needs.
Engineering
From concept and design to engineering and automation, built for execution, compliance, and real-world performance.
Quality & Documentation
Complete validation documentation supporting GMP and IQ/OQ/PQ qualification processes.
Manufacturing
High-capacity production of tanks, vessels, piping, skids and process units, CIP and utility systems.
Installation & Commissioning
Coordinated on-site execution from factory to operation.
Service & Lifecycle Support
Ongoing lifecycle support ensuring stable operation, and compliance.
Rebuilds & Upgrades
Upgrades, modifications, and rebuilds of existing facilities – executed with minimal disruption.
Pharma project model
We engage at any phase and deliver across all.
The project model follows ISPE guidelines, covering every phase from Concept Design through Process Qualification. We engage for the full delivery or for the specific phases as needed.
CD
Concept Design
Developing a new idea to visualize, brainstorm and refine into a preliminary, high-level design.
BD
Basic Design
Defining the overall scope to gather quotes, including tank sizes and system numbers.
DD
Detailed Design
Finalizing designs with detailed documents, such as isometrics and parts lists, ready for manufacturing.
DQ
Design Qualification
Client verifies the design meets specified requirements, greenlighting production.
FAB
Fabrication
Building the process equipment as per detailed designs.
FAT
Factory Acceptance Test
Review of the product and documentation before leaving the factory.
SAT
Site Acceptance Test
On-site verification of the installed equipment and its documentation by the client.
IQ
Installation Qualification
Verification that all physical installations are correctly connected and assembled.
OQ
Operational Qualification
Testing control systems and automation, ensuring everything functions as expected.
PQ
Process Qualification
Performing a full production run test to validate the process equipment with a designed medium.
SV
Service
Maintenance and scheduled service to ensure uptime, extend equipment life, and support clients throughout the lifecycle.
AM
Aftermarket
Supplying spare parts, upgrades, and retrofits to keep equipment up to date with standards and client needs.
Quality & Documentation
Quality that secures compliance and traceability
Stainless-steel process skids and installations built for regulated environments.
Built to meet pharmaceutical requirements for traceability, validated documentation, and hygienic performance ensuring compliance, reliability, and long-term audit readiness.
Capacity & Delivery
Capacity to deliver at scale.
Complete process systems delivered with the capacity to handle large and complex projects.
A scalable setup and strong manufacturing capabilities enable parallel execution, high throughput, and reliable delivery — even in demanding project environments.
Supported by multiple locations and scalable resources across Europe.
Let's create better solutions together
Contact us.
Rene Dyrlund
Senior Technical Sales & Construction Manager - Kalundborg
High-capacity execution at scale
