Services > Cleanroom engineering
Pharmaceutical cleanrooms
Ensuring compliance and sterility for pharmaceutical manufacturing
We specialize in the design, supply, installation, construction, and maintenance of pharmaceutical cleanroom systems. Our cleanrooms are engineered to meet the stringent requirements for sterility and compliance, ensuring optimal conditions for pharmaceutical production.
Overview
Ensuring a sterile environment is paramount in pharmaceutical manufacturing. BNQ Engineering provides comprehensive cleanroom solutions that adhere to the strictest standards of cleanliness and regulatory compliance. Our pharmaceutical cleanrooms are designed to prevent contamination, protect product integrity, and comply with GMP, FDA, and ISO 14644 standards. We deliver turnkey solutions that support the entire lifecycle of your cleanroom, from design and construction to certification and maintenance.
Key features
- Compliance with GMP, FDA standards, and ISO 14644
- Certification in accordance with NEBB (IEST procedures) and ISO 14644-2
- Tailored solutions for Class 1 to Class 100K cleanrooms
- Advanced contamination control and environmental monitoring
Our services and process
Compliance and safety
Our pharmaceutical cleanrooms comply with industry standards such as GMP, FDA, and ISO 14644. We prioritize safety in all our projects, adhering to strict safety standards to protect both personnel and equipment.
Benefits and value proposition
Sterile environments
Our pharmaceutical cleanrooms provide the sterile conditions necessary for safe and compliant pharmaceutical production.
Compliance
Our cleanrooms comply with GMP, FDA, and ISO 14644 standards, ensuring high-quality and reliable operation.
Quality
We prioritize quality in every aspect of our cleanroom construction, from materials and workmanship to final certification.
Custom solutions
We offer tailored cleanroom solutions that meet the unique needs of the pharmaceutical industry, ensuring optimal performance and compliance with industry standards.