Cleanroom Panel is a high-performance modular wall and ceiling system specially designed for cleanroom environments. It provides a smooth, hygienic, and durable surface that meets the strict requirements of pharmaceutical manufacturing, laboratories, hospitals, biotechnology facilities, electronics factories, and food processing plants.

Manufactured with high-quality steel sheets and various core materials such as rock wool, PIR, PU, honeycomb, or magnesium oxide, cleanroom panels offer excellent thermal insulation, fire resistance, sound insulation, and easy installation. The modular design allows for quick assembly, maintenance, and future expansion.

Pharma United cleanroom panels are available in multiple surface finishes, including PPGI, HPGI, HPL, and VCM-coated steel, ensuring compliance with GMP, ISO, and cleanroom standards.

Product Types
Cleanroom Doors — Includes swing doors, sliding doors, and hermetic (airtight) doors, available in single-leaf and double-leaf configurations
Cleanroom Windows — Includes fixed observation windows and vision panels for wall-mounted viewing between cleanroom zones
Air Shower Doors / Pass-Through Windows — Specialized units for material and personnel transfer between clean and non-clean areas

Key Features
Sealed, flush surfaces — Smooth, gap-free construction minimizes dust accumulation and particle shedding
Airtight sealing — Rubber or silicone gaskets maintain pressure differentials between cleanroom zones (critical for ISO Class 5-8 environments)
Corrosion-resistant materials — Typically constructed from powder-coated steel, stainless steel, or aluminum honeycomb panels for durability and easy cleaning
Fire-rated options — Available in various fire resistance ratings for facilities requiring code compliance
Antistatic and antibacterial finishes — Optional coatings for electronics or medical-grade cleanrooms

Common Applications
Pharmaceutical manufacturing facilities
Semiconductor and electronics cleanrooms
Hospital operating rooms and sterile processing areas
Biotechnology and research laboratories
Food and beverage sterile production lines

Key Features
Contamination control — Equipment designed to minimize particle generation, shedding, and accumulation throughout the facility
Sealed, cleanable surfaces — Smooth, non-porous materials that resist microbial growth and simplify disinfection procedures
Pressure and airflow management — Systems engineered to maintain positive or negative pressure differentials between adjacent zones and prevent cross-contamination
Compliance-oriented design — Built to support ISO 14644, GMP, and FDA facility requirements, with materials and construction suited to regular validation and audit processes

Common Applications
Pharmaceutical and biotechnology manufacturing
Semiconductor and electronics fabrication
Hospital operating rooms and sterile compounding pharmacies
Food and beverage aseptic production lines
Medical device assembly and packaging

Key Features
Prefabricated construction — Built and quality-tested in a factory setting, reducing on-site construction time and minimizing contamination risk during installation
Rapid deployment — Units can typically be installed and operational significantly faster than conventional cleanroom builds, often in weeks rather than months
Modular scalability — Individual PODs can be added, reconfigured, or relocated to accommodate changing production volumes or facility layouts
Self-contained environmental control — Integrated HVAC, filtration, and pressure control systems allow PODs to maintain specific ISO cleanliness classes independently or as part of a larger facility system
Sealed, cleanable enclosure — Smooth interior surfaces and airtight panel joints support consistent particle control and ease of sanitation

Common Applications
Pharmaceutical and biotechnology manufacturing requiring flexible or phased capacity expansion
Temporary or emergency-response production and testing facilities
Semiconductor and electronics cleanroom deployments in space-constrained facilities
R&D and pilot-scale production environments where reconfiguration is frequent
Facilities retrofitting cleanroom capability into existing buildings without major structural renovation