Expert Cleanroom Services for Critical Industries
Nordic Clean Tech delivers comprehensive cleanroom validation, qualification and training services that ensure regulatory compliance, operational excellence, and manufacturing confidence across all high-tech industries — From semiconductors to pharmaceuticals, medical devices to aerospace, food processing to battery manufacturing.
🏆
30+ years industry expertise
GMP, FDA, ISO 14644. Cleanroom validation & qualification across critical sectors.
🤖
AI-driven 40% Faster
Automated documentation & intelligent compliance streamline your validation process.
📄
Audit-Ready Delivery
Documented and compliant, ready for regulators and quality inspections.
🌍
Multi-sector Leadership
Pharma, electronics, food, battery, medical, aerospace, robotics & more.
📞
Direct Expert Access
Fast, personal support. Custom approach for your environment.
Our Services
Cleanroom Qualification
Comprehensive ISO 14644 and GMP qualification for all environments.
-
Design & system review
-
Installation/operational qualification
-
Environmental monitoring
Regulatory Validation
GDP, GMP, FDA, ISO compliant solutions.
-
Validation master plans (VMP)
-
Equipment & process validation
-
Audit-prep & gap analysis
Training & Consulting
Employee & manager training on cleanroom operation & compliance.
-
ISO standards training
-
Custom workshops
- Best practices adoption
Automated Documentation
Accelerate reporting and compliance with our smart systems.
-
Live compliance dashboards
- Automated reporting
Start Project
From commissioning to repurposing existing facilities.
-
Site assessment
-
Pilot runs & troubleshooting
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
30+
Years of Specialised Experience
Over three decades dedicated exclusively to cleanroom qualifications, validation, commissioning and troubleshooting across pharmaceutical, electronics, medical device, food, aerospace, robotics and emerging industries
40%
Timeline Reduction
AI-supported innovation reduces validation timelines whilst maintaining full regulatory compliance
Compleat
Audit-Ready Documentation
Two decades dedicated exclusively to cleanroom qualification and process validation across pharmaceutical, electronics, medical device, food, aerospace, and emerging industries
Revolutionary AI-Supported qualification & Validation Services
NCT CleanTech Quoter: Launching February 2026
Our qualification and validation processes revolutionise cleanroom qualification through automated documentation, intelligent testing protocols, and up-to-date compliance measuring protocols supported by AI-Team across all industries.
This first-to-market AI-supported qualification and validation tool reduces project timelines up to 40% whilst maintaining rigorous regulatory standards. The system generates for example industry-specific qualification protocols, automates documentation workflows, generates intelligent and timewise tasks, 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, repurposing existing facilities, or need process validation, Nordic Clean Tech delivers the qualification and 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.