Regulated by FDA in the United States and EMA in Europe, Pharmaceutical cleanrooms are required to meet CGMP (Current Good Manufacturing Practice) standards for safety and quality. If a pharmaceutical cleanroom follows CGMP standards, it assures strength, quality, identity, and purity, needed by manufacturers.
To put in simple words, GMP assures consistent quality and safety of all the products. Safety is dependent on 5 main elements- people, premises, processes, products and procedures.
These pharmaceutical cleanrooms by Zeibaq are used by manufacturers all across Saudi Arabia. We are known for quality products and post installation services as well. Zeibaq’s pharmaceutical cleanrooms are 100/ISO5. However, we also have cleanrooms that are slightly lower in classification, depending on the budget of our clients and their business needs.
Below-mentioned are different components of pharmaceutical cleanrooms manufactured by Zeibaq
Temperature and humidity control
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.
Due to regular use of harsh chemicals for cleaning, only Finer Reinforced Plastic (FRP) walls are used as it has excellent chemical resistance. oms support drug formulation, sterile filling, packaging, quality control, and laboratory operations requiring strict contamination control.
Commonly pharmaceutical cleanrooms use chemical resistant flooring . This is because the powerful cleaning chemicals used in pharmaceutical cleanrooms are so aggressive that they will end up damaging the regular floor. The most common type of flooring is heat-welded vinyl with epoxy coating and urethane over coat.
Current Good Manufacturing Practices (CGMP) is the FDA-mandated safety standard that all pharmaceutical cleanrooms have to adhere to. CGMP is basically a higher standard than Good Manufacturing Practices (GMP).
A pharmaceutical cleanroom is an ISO-5/class 100 for aseptic filling and sterile process.
A pharmaceutical cleanroom is an enclosed room that is used to manufacture medicines. These cleanrooms must follow FDA guidelines to ensure safety and effectiveness of the medicine. Cleanrooms not only require highly sterile environments but also top-notch level cleanliness.
Pharmaceutical cleanrooms need both- viable and non-viable particle testing.
A buffer room is a classified room in a cleanroom that is designed to prevent cross-contamination. It is usually used for less critical functions such as staging, preparing vials, etc.
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