Asegure el arranque de su planta: OPEX cero en mantenimiento durante 12 meses - Solicítelo al formalizar su proyecto de Entorno Controlado durante este semestre, asumimos el 100% de la bonificación del plan de mantenimiento preventivo del primer año. Garantía de uptime y cumplimiento normativo.Asegure el arranque de su planta: OPEX cero en mantenimiento durante 12 meses - Solicítelo al formalizar su proyecto de Entorno Controlado durante este semestre, asumimos el 100% de la bonificación del plan de mantenimiento preventivo del primer año. Garantía de uptime y cumplimiento normativo.

Mercados

5 mercados. 31 sectores. 12 familias de Entornos Controlados. Un equipo de ingeniería que comprende las diferencias entre ellos y las conexiones que los hacen funcionar juntos.

Farmacéutico e Industria API

Farmacéutico e Industria API

Grade D to Grade A — every GMP class, every regulatory framework, a single project owner.

Hospitals & Clinical Centres

Hospitals & Clinical Centres

Sterile preparation, isolation rooms, nuclear medicine — built in active clinical environments without interrupting patient care.

Medical Devices

Medical Devices

MDR 2017/745, FDA QMSR, ISO 13485 — classified environments built to pass the Notified Body and FDA with the same documentation package.

Biotechnology & R&D

Biotechnology & R&D

From BSL-1 laboratories to GMP biomanufacturing suites — one partner across the full development arc.

In Vitro Diagnostics (IVD)

In Vitro Diagnostics (IVD)

The IVDR raised the bar on manufacturing controls. The compliance gap is a facility gap.

Veterinary

Veterinary

Live pathogens. Pharmaceutical GMP. Both in the same facility — resolved by a single engineering team.

Medicinal Cannabis

Medicinal Cannabis

Same GMP as conventional pharmaceutical. Same inspections. No shortcuts in a regulated medicinal product manufacturing environment.

Advanced Therapy Medicinal Products (ATMP)

Advanced Therapy Medicinal Products (ATMP)

Grade A with containment. GMP with biosafety. The intersection no conventional cleanroom contractor can resolve alone.

Food & Beverage

Food & Beverage

Distribution audit readiness, FSMA compliance and aseptic filling — physical controls built where product safety is the brand.

Nutraceuticals

Nutraceuticals

GMP expectations from pharmaceutical clients. Food safety regulation from the authorities. One facility that satisfies both.

Cosmetics & Consumer Care

Cosmetics & Consumer Care

Regulation EC 1223/2009, ISO 22716 — cosmetic GMP environments built for the Responsible Person and the next retail audit.

Foodtech

Foodtech

Precision fermentation and cellular agriculture demand pharmaceutical-grade environmental controls. Most food-sector builders cannot deliver them.

Semiconductors

Semiconductors

El rendimiento de fabricación es función directa del control ambiental. Cada decisión de diseño tiene un coste de producción.

Batteries & Energy Storage

Batteries & Energy Storage

Dew point −55°C. Any humidity deviation is a defective cell and a safety event. Simultaneously.

Photovoltaics

Photovoltaics

Surface cleanliness determines conversion efficiency. Humidity during lamination determines module service life.

Microelectronics

Microelectronics

Optical components, precision sensors, advanced electronics — environments where surface cleanliness determines product performance.

Automotive

Automotive

EV components, ADAS sensors, power electronics — electrification created cleanroom requirements that conventional automotive facilities cannot cover.

Data Centres

Data Centres

Availability is not a feature. It is the product. The environment that guarantees it is precision engineering.

Aerospace

Aerospace

Outgassing. Molecular contamination. Vibration. The three variables that determine whether a satellite works in orbit — and whether it can be assembled on the ground.

Advanced Manufacturing

Advanced Manufacturing

Reactive metal powders, precision composites, MEMS — the atmosphere is a process variable that must be engineered.

Aviation

Aviation

Critical flight components. AS9100 quality system. The environment is where compliance is physically materialised.

Fine Chemicals & Specialities

Fine Chemicals & Specialities

Pharmaceutical-grade purity. Industrial-scale economics. High-potency containment where both are simultaneously required.

Biocides & Agrochemicals

Biocides & Agrochemicals

Since 2022, surgical antiseptics are pharmaceutical GMP — not biocides. The facility requirement changed without adequate notice to many manufacturers.

Defence

Defence

Contamination control. Physical security. EMI shielding. In defence manufacturing, all three are mission requirements — not independent workstreams.

Nanotechnology

Nanotechnology

Sub-100nm particles are simultaneously the product and the contamination risk. Conventional cleanroom filtration does not address either.

Biosafety BSL-2 / BSL-3

Biosafety BSL-2 / BSL-3

Secondary containment for serious infectious disease research — designed for the consequences of agent failure, not a generic standard.

Heritage Conservation

Heritage Conservation

There are objects that cannot be replaced. The environment that preserves them cannot fail — ever.

Research Centres & Universities

Research Centres & Universities

A cleanroom built for a five-year programme must remain qualifiable for the next one. We design for the research lifecycle.

Nuclear Medicine & Radiopharmacy

Nuclear Medicine & Radiopharmacy

PET, SPECT, theranostics — the fastest-growing pharmaceutical manufacturing segment requires the most complex integration of facilities.

Biobanks & Precision Medicine

Biobanks & Precision Medicine

The sample is irreplaceable. The storage system must be designed knowing that.

Metrology, Calibration & Testing

Metrology, Calibration & Testing

Vibration at nanometre scale. Thermal drift at thousandths of a degree. The measurement is only as good as the environment in which it is made.