Entornos Controlados
ISO/IEC 17025 · GMP · Quality control · Analytical · R&D
Laboratories for analytical chemistry, quality control, and R&D, specified from the science outward.
En detalle
The laboratory is where quality is demonstrated, not assumed. We design precision laboratories for analytical chemistry, quality control and R&D: HVAC sized for gas extraction loads, integration of biological safety cabinets, environmental stability demanded by the measurement method. 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 accordance with Annex 15, and institutional biosafety frameworks. Within GMP facilities they function 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, a single project owner.
See more →Sectores aplicables
MDR 2017/745, FDA QMSR, ISO 13485 — classified environments built to pass the Notified Body and FDA with the same documentation package.
See more →Sectores aplicables
Live pathogens. Pharmaceutical GMP. Both in the same facility — resolved 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 must be engineered.
See more →Sectores aplicables
Sub-100nm particles are simultaneously the product and the contamination risk. Conventional cleanroom filtration does not address either.
See more →Sectores aplicables
PET, SPECT, theranostics — the fastest-growing pharmaceutical manufacturing segment requires the most complex integration of facilities.
See more →Sectores aplicables
Grade D to Grade A — every GMP class, every regulatory framework, a single project owner.
See more →Sectores aplicables
MDR 2017/745, FDA QMSR, ISO 13485 — classified environments built to pass the Notified Body and FDA with the same documentation package.
See more →Sectores aplicables
Live pathogens. Pharmaceutical GMP. Both in the same facility — resolved 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 must be engineered.
See more →Sectores aplicables
Sub-100nm particles are simultaneously the product and the contamination risk. Conventional cleanroom filtration does not address either.
See more →Sectores aplicables
PET, SPECT, theranostics — the fastest-growing pharmaceutical manufacturing segment requires the most complex integration of facilities.
See more →Sectores aplicables
Grade D to Grade A — every GMP class, every regulatory framework, a single project owner.
See more →Sectores aplicables
MDR 2017/745, FDA QMSR, ISO 13485 — classified environments built to pass the Notified Body and FDA with the same documentation package.
See more →Sectores aplicables
Live pathogens. Pharmaceutical GMP. Both in the same facility — resolved 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 must be engineered.
See more →Sectores aplicables
Sub-100nm particles are simultaneously the product and the contamination risk. Conventional cleanroom filtration does not address either.
See more →Sectores aplicables
PET, SPECT, theranostics — the fastest-growing pharmaceutical manufacturing segment requires the most complex integration of facilities.
See more →Sectores aplicables
Preservation environments for museums and archives, with stable temperature and humidity plus continuous monitoring.
