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Industry Solutions
Every industry has unique contamination control and regulatory requirements.
Nordic Clean Tech provides specialised cleanroom validation programs tailored for each manufacturing sector, ensuring full compliance, performance reliability, and audit-ready documentation.
We serve multiple high-tech industries, including:
Pharmaceuticals & Biotechnology – GMP Annex 1-compliant validation for sterile drug manufacturing and biologics production.Electronics & Semiconductors – ISO Class 1-5 validation with sub-micron particle control and electrostatic discharge protection.
Medical Devices – ISO 13485 qualification for implantable and diagnostic device manufacturing.
Battery Manufacturing – Ultra-dry cleanroom validation for lithium-ion cell assembly and electrode processing.
Food Processing – FDA cGMP and FSSC 22000-compliant validation for hygienic production and packaging.
Aerospace & Defence – Mission-critical validation for satellite, optical, and propulsion component manufacturing.
Our team understands that no two facilities are the same.
We adapt testing protocols, documentation, and qualification phases to fit your specific environment — delivering regulatory-approved performance across all critical manufacturing industries.