We design, build and maintain cleanrooms for the biopharmaceutical sector, ensuring stable environmental conditions and full GMP compliance.
We develop integrated solutions tailored to each process, defining the most appropriate technical configuration in each case.
What we deliver
Our solutions enable precise control of temperature, humidity, differential pressure and particle concentration, ensuring suitable environments for critical pharmaceutical processes.
We deliver complete installations for production, filling, distribution and storage, minimising the risk of cross-contamination and ensuring microbiological control.
Problem it solves
Each project is developed with a system-level approach, integrating architectural layout, pharmaceutical HVAC and process equipment. Particular attention is given to ensuring specific environmental conditions at every stage of the pharmaceutical process.
Temperature, humidity, differential pressure and particle concentration must remain within defined parameters to ensure process validity and product quality.
A properly designed and executed system enables →
- Operate under stable and controlled conditions
- Reduce the risk of cross-contamination
- Ensure sterile and aseptic processes
- Comply with GMP requirements
- Adapt the environment to the production process
Up to 40% reduction in energy overconsumption through proper system sizing and control
What we can deliver
MODULAR ARCHITECTURE
We define cleanroom architecture through modular systems integrating wall panels, ceilings, flooring, windows and doors. This configuration structures the space, allows integration of installations and auxiliary equipment, and ensures compliance with regulatory and quality standards.
HVAC SYSTEMS
We design HVAC systems specifically for pharmaceutical environments, focused on precise control of temperature, humidity, differential pressure and particle concentration. The system is defined as a core element of the facility, ensuring environmental stability and reducing contamination risks.