LABORATORIES
Laboratories built for precision, compliance and workflow.
Laboratories are complex, regulated environments where analytical precision, contamination control, safety and regulatory compliance must all be achieved simultaneously. Iberconcept designs and delivers complete laboratory environments, from QC labs and stability testing areas to R&D spaces and microbiology suites, where every system is coordinated and specified for the laboratory's exact requirements.
With over 20 years of experience in pharmaceutical projects across more than 30 countries, Iberconcept ensures that every laboratory we deliver meets GLP, GMP and ISO standards, designed for the workflow, validated for the process and ready for regulatory inspection from day one.
Solutions for Laboratories
Each card below represents a key discipline in the design and delivery of laboratories. Click to explore the systems, components and products Iberconcept integrates within each category.
About Iberconcept
Iberconcept is an international reference in the design, engineering and delivery of integrated solutions for the pharmaceutical industry — cleanrooms, laboratories and controlled production environments.
With an integrated portfolio covering modular construction, HVAC, electrical systems, medical gases, fire protection and specialist equipment, Iberconcept acts as a single point of contact from initial consulting through to final handover, ensuring quality, compliance and reliability in every project.
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Key Questions about Pharmaceutical Laboratories
What cleanroom solutions does Iberconcept provide for the pharmaceutical industry?
Iberconcept provides turnkey pharmaceutical cleanroom solutions, covering design, engineering, modular construction, HVAC systems, electrical systems, fire protection and specialised equipment for regulated manufacturing environments.
Which pharmaceutical cleanroom classifications does Iberconcept support?
Iberconcept designs cleanrooms according to ISO cleanroom classifications and GMP requirements, supporting different grades and process-specific contamination control needs.
How are pharmaceutical cleanrooms designed to meet GMP requirements?
Cleanrooms are designed with controlled airflow, high-efficiency filtration, pressure differentials and validated materials, ensuring compliance with GMP regulations throughout the facility lifecycle.
What role does HVAC play in pharmaceutical cleanrooms?
HVAC systems are critical for air filtration, laminar airflow, pressure control, temperature and humidity stability, directly supporting product quality and regulatory compliance.
Can Iberconcept cleanrooms be customised for specific pharmaceutical processes?
Yes. Iberconcept develops customised cleanroom solutions adapted to manufacturing processes such as sterile production, compounding, filling or packaging.
Are modular construction systems suitable for pharmaceutical cleanrooms?
Yes. Modular construction allows fast installation, hygienic finishes, easy cleaning and future adaptability, making it ideal for pharmaceutical cleanrooms.
What equipment is typically integrated into pharmaceutical cleanrooms?
Integrated equipment may include pass boxes, air showers, workstations, cabinets and monitoring systems, all selected to support cleanroom workflows and compliance.
Can pharmaceutical cleanrooms be expanded or upgraded?
Yes. Iberconcept cleanrooms are designed for future expansion or reconfiguration, minimising downtime during facility upgrades.
Does Iberconcept deliver pharmaceutical cleanrooms worldwide?
Yes. Iberconcept delivers pharmaceutical cleanroom projects worldwide, supporting global manufacturers with consistent quality and regulatory compliance.
