Controlled Environments
ISO/IEC 17025 · GMP · Quality control · Analytics · R&D
Laboratories for analytical chemistry, quality control and R&D, with specifications that start from the science.
In detail
The laboratory is where quality is demonstrated, not where it is assumed. We design precision laboratories for analytical chemistry, quality control and R&D: HVAC sized for fume extraction loads, integration of biological safety cabinets, the environmental stability the measurement method demands. The specification starts from the science — not from a generic equipment catalogue.
Our laboratories support ISO/IEC 17025:2017 accreditation under ENAC (Spain), GMP qualification in line with Annex 15 and institutional biosafety frameworks. Within GMP facilities they operate as integral components of the quality system. Every analytical result generated in an Enforced facility is traceable to the environment that produced it.
Grade D to Grade A — every GMP class, every regulatory framework, one single project owner.
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MDR 2017/745, FDA QMSR, ISO 13485 — classified environments built to pass both the Notified Body and the FDA with the same documentation package.
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Live pathogens. Pharmaceutical GMP. Both in the same facility — solved by a single engineering team.
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Precision fermentation and cellular agriculture demand pharmaceutical-grade environmental controls. Most food-sector builders cannot deliver them.
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Reactive metal powders, precision composites, MEMS — the atmosphere is a process variable that has to be engineered.
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Sub-100nm particles are simultaneously the product and the contamination risk. Conventional cleanroom filtration addresses neither.
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PET, SPECT, theranostics — the fastest-growing pharmaceutical manufacturing segment demands the most complex facility integration.
See more →Sectores aplicables
Grade D to Grade A — every GMP class, every regulatory framework, one single project owner.
See more →Sectores aplicables
MDR 2017/745, FDA QMSR, ISO 13485 — classified environments built to pass both the Notified Body and the FDA with the same documentation package.
See more →Sectores aplicables
Live pathogens. Pharmaceutical GMP. Both in the same facility — solved by a single engineering team.
See more →Sectores aplicables
Precision fermentation and cellular agriculture demand pharmaceutical-grade environmental controls. Most food-sector builders cannot deliver them.
See more →Sectores aplicables
Reactive metal powders, precision composites, MEMS — the atmosphere is a process variable that has to be engineered.
See more →Sectores aplicables
Sub-100nm particles are simultaneously the product and the contamination risk. Conventional cleanroom filtration addresses neither.
See more →Sectores aplicables
PET, SPECT, theranostics — the fastest-growing pharmaceutical manufacturing segment demands the most complex facility integration.
See more →Sectores aplicables
Grade D to Grade A — every GMP class, every regulatory framework, one single project owner.
See more →Sectores aplicables
MDR 2017/745, FDA QMSR, ISO 13485 — classified environments built to pass both the Notified Body and the FDA with the same documentation package.
See more →Sectores aplicables
Live pathogens. Pharmaceutical GMP. Both in the same facility — solved by a single engineering team.
See more →Sectores aplicables
Precision fermentation and cellular agriculture demand pharmaceutical-grade environmental controls. Most food-sector builders cannot deliver them.
See more →Sectores aplicables
Reactive metal powders, precision composites, MEMS — the atmosphere is a process variable that has to be engineered.
See more →Sectores aplicables
Sub-100nm particles are simultaneously the product and the contamination risk. Conventional cleanroom filtration addresses neither.
See more →Sectores aplicables
PET, SPECT, theranostics — the fastest-growing pharmaceutical manufacturing segment demands the most complex facility integration.
See more →Sectores aplicables
