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Precise Cleanroom Validation Across Critical Manufacturing Industries
From semiconductors to pharmaceuticals, medical devices to aerospace, food processing to battery manufacturing—Nordic Clean Tech delivers comprehensive cleanroom validation services and training that ensure regulatory compliance, operational excellence, and manufacturing confidence across all high-tech industries.
20 Years of GMP & ISO 14644 Excellence
At Nordic Clean Tech, we understand that pharmaceutical, biotech, medical device, high-tech electronics, and advanced manufacturing demand the highest standards of environmental control. Our cleanroom validation services ensure your facilities meet and exceed stringent GMP, FDA, ISO 14644, and industry-specific standards.
With over two decades of specialised experience, we bring Nordic precision and engineering excellence to every qualification and validation project. Our comprehensive approach combines advanced testing methodologies, detailed documentation, and strategic consulting to deliver cleanroom environments that perform reliably under the most demanding conditions.
Comprehensive Industry Solutions
High-Tech Electronics
ISO Class 1-5 validation for semiconductor fabs, MEMS manufacturing, and photonics production with sub-micron particle control
Pharmaceutical & Biotech
GMP Annex 1 compliant validation for sterile drug manufacturing, biologics production, and cell therapy facilities
Medical Devices
ISO 13485 validation for implantable devices, diagnostic equipment, and surgical instrument manufacturing
Battery Manufacturing
Specialised dry room validation for lithium-ion battery production with ultra-low humidity control
Food Processing
FDA cGMP and FSSC 22000 compliant validation for sterile packaging and functional food production
Aerospace & Defence
Mission-critical validation for satellite components and space hardware manufacturing
Why Nordic Clean Tech Leads the Industry
When selecting a cleanroom partner, experience and precision matter. Nordic Clean Tech combines deep technical expertise across multiple industries, comprehensive regulatory knowledge, and client-focused service delivery to exceed expectations on every project.
Our team has successfully built cleanrooms ranging from 3m² to 10,000m², serving clients across Europe and the Middle East. This breadth of experience ensures we understand the unique challenges of each industry sector and deliver solutions tailored to your specific requirements.
Our Validation Expertise by the Numbers
20+
Years Specialised Experience
Two decades dedicated exclusively to cleanroom validation across pharmaceutical, electronics, medical device, food, aerospace, and emerging industries
40%
Timeline Reduction
AI-supported innovation reduces validation timelines from 12-24 months to 7-12 months whilst maintaining full regulatory compliance
Compleat
Audit-Ready Documentation
Two decades dedicated exclusively to cleanroom validation across pharmaceutical, electronics, medical device, food, aerospace, and emerging industries
Revolutionary AI-Supported Validation Services
NCT CleanTech Quoter: Launching February 2026
Our validation process revolutionises cleanroom qualification through automated documentation, intelligent testing protocols, and real-time compliance monitoring supported by AI-Team across all industries.
This first-to-market AI supported validation tool reduces project timelines up to 40% whilst maintaining rigorous regulatory standards. The system generates industry-specific validation protocols, automates documentation workflows, and provides continuous compliance tracking.
Partner with NCT Multi-Industry Cleanroom Validation Experts
Whether you're commissioning a new semiconductor fab, pharmaceutical facility, medical device cleanroom, battery manufacturing plant, food processing facility, or aerospace production area, Nordic Clean Tech delivers the validation expertise you need for success.
Our team is ready to discuss your cleanroom validation requirements across any industry and develop a customised approach that ensures regulatory compliance, operational excellence, and manufacturing confidence.