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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

1

Consultation

We start with an in-depth consultation to understand your specific cleanroom requirements. This includes site assessments, understanding your operational needs, and discussing compliance requirements.
2

Design and planning

Our cleanroom design services are tailored to meet the unique needs of the pharmaceutical industry. We create detailed plans and schematics that adhere to GMP, FDA, and ISO 14644 standards, ensuring optimal environmental conditions.
3

Supply

We source high-quality components and equipment necessary for your cleanroom construction. Our supply chain partnerships enable us to provide reliable and cutting-edge technology that meets industry standards.
4

Installation and construction

Our skilled team handles all aspects of cleanroom construction and installation, ensuring that your cleanroom is built to the highest standards of quality and compliance. We integrate mechanical, electrical, and plumbing systems to support the cleanroom environment.
5

Certification and commissioning

We conduct thorough testing and commissioning to ensure your cleanroom meets all performance criteria. Our certification processes adhere to NEBB (IEST procedures) and ISO 14644-2, guaranteeing that your cleanroom operates within the required parameters for cleanliness and environmental control.
6

Maintenance and support

We offer ongoing maintenance and support services to keep your cleanroom operating at peak efficiency. Our services include regular inspections, preventive maintenance, and prompt repairs to address any issues that arise.

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.

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