Secure your plant start-up: zero maintenance OPEX for 12 months - Request it when you finalize your Controlled Environment project this half-year, and we will cover 100% of the first-year preventive maintenance plan. Guaranteed uptime and regulatory compliance.Secure your plant start-up: zero maintenance OPEX for 12 months - Request it when you finalize your Controlled Environment project this half-year, and we will cover 100% of the first-year preventive maintenance plan. Guaranteed uptime and regulatory compliance.

Markets

5 markets. 31 sectors. 12 families of Controlled Environments. An engineering team that understands the differences between them and the connections that make them work together.

Pharmaceutical and API Industry

Pharmaceutical and API Industry

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

Hospitals and Clinical Centres

Hospitals and Clinical Centres

Sterile compounding, isolation rooms, nuclear medicine — built in live clinical environments without interrupting care.

Medical Devices

Medical Devices

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

Biotechnology and R&D

Biotechnology and R&D

From BSL-1 laboratories to GMP biomanufacturing suites — a single partner across the whole development arc.

In Vitro Diagnostics (IVD)

In Vitro Diagnostics (IVD)

The IVDR tightened manufacturing controls. The compliance gap is a facilities gap.

Veterinary

Veterinary

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

Medical Cannabis

Medical Cannabis

The same GMP as conventional pharma. The same inspections. There are no shortcuts in a regulated medicines 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 solve alone.

Food and Beverage

Food and Beverage

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

Nutraceuticals

Nutraceuticals

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

Cosmetics and Consumer Care

Cosmetics and 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

Manufacturing yield is a direct function of environmental control. Every design decision carries a production cost.

Batteries and Energy Storage

Batteries and 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 meet.

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 has to be engineered.

Aviation

Aviation

Flight-critical components. AS9100 quality system. The environment is where compliance takes physical form.

Fine and Specialty Chemicals

Fine and Specialty Chemicals

Pharmaceutical-grade purity. Industrial-scale economics. High-potency containment where both are needed at once.

Biocides and Plant Protection Products

Biocides and Plant Protection Products

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

Defence

Defence

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

Nanotechnology

Nanotechnology

Sub-100nm particles are simultaneously the product and the contamination risk. Conventional cleanroom filtration addresses neither.

BSL-2 / BSL-3 Biosafety

BSL-2 / BSL-3 Biosafety

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

Heritage Conservation

Heritage Conservation

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

Research Centres and Universities

Research Centres and Universities

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

Nuclear Medicine and Radiopharmacy

Nuclear Medicine and Radiopharmacy

PET, SPECT, theranostics — the fastest-growing pharmaceutical manufacturing segment demands the most complex facility integration.

Biobanks and Precision Medicine

Biobanks and Precision Medicine

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

Metrology, Calibration and Testing

Metrology, Calibration and Testing

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