Ziebaq delivers advanced controlled-environment cleanrooms designed for pharmaceutical, biotechnology, and high-precision manufacturing applications. Our systems support both certified and non-certified areas, including ISO 5, ISO 7, ISO 8, and CNC classifications, and are fully aligned with global cGMP requirements and international cleanroom standards.
Ziebaq modular cleanroom systems are engineered to maintain the highest levels of contamination control, operational safety, and compliance—ideal for environments handling sensitive formulations, sterile products, and high-potency materials.
Premium Material Construction
Our cleanrooms are built using high-performance materials with excellent mechanical resistance, ensuring durability and full compatibility with rigorous disinfection and cleaning procedures commonly used in pharmaceutical settings.
Superior Finishes & Hygienic Design
Ziebaq systems are designed with flawless finishes, seamless joints, and hygienic detailing to minimise particle accumulation. This ensures a pristine environment while enhancing your facility’s professionalism and readiness for audits, client visits, and regulatory inspections.
Modular Flexibility & Turnkey Expertise
With deep expertise in modular cleanroom engineering, Ziebaq offers flexible layouts, rapid installation, and complete turnkey delivery. Our end-to-end approach provides a reliable single point of contact—ideal for both compact labs and large-scale production plants.
Advanced HVAC & Filtration Technology
Our cleanroom HVAC systems integrate HEPA and ULPA filtration, pressure cascade design, and airflow optimisation supported by Computational Fluid Dynamics (CFD) analysis. This ensures compliance with global standards while protecting both operators and products at every stage of processing.
Ziebaq cleanrooms support drug formulation, sterile filling, packaging, quality control, and laboratory operations requiring strict contamination control.
Ziebaq cleanrooms align with ISO classifications, GMP guidelines, and international pharmaceutical regulatory standards.
Yes, Ziebaq designs cleanrooms for both sterile and non-sterile pharmaceutical processes, tailored to specific risk levels.
Ziebaq modular systems allow pharmaceutical companies to expand cleanrooms efficiently as production demands grow.
Ziebaq delivers fully integrated turnkey solutions, coordinating design, systems, installation, and commissioning for pharmaceutical facilities.
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