Fire Safety Priority
Solves: Fire code overrides all other considerations
High Cleanliness & Fire Rated
Solves: Non-combustible fire safety, cleanliness and solid structural strength are all required
Thermal Insulation
Solves: Economic advantages than rockwool and magnesium systems
Lightweight Rigidity
Solves: Structural load limits and fast installation
Hygiene & Durability
Solves: Maintenance concerns and surface-lifecycle decision
Precision Manufacturing
Solves: Inconsistent quality
High Load & Airtight
Solves: Structural sagging in large cleanrooms & High cost of future renovations
Airflow Control
Solves: Uneven air distribution
Flexible & Modular
Solves: Enables flexible cleanroom modifications and hidden service routing without breaking walls or disrupting operations
Pressure Integrity
Solves: Pressure leakage and cross-zone contamination in critical environments
Traffic Control
Solves: Space constraints in compact cleanroom layouts
Fire–GMP Balance
Solves: Fire safety compliance without compromising cleanroom integrity
Hygiene Control
Solves: Material degradation and hygiene failure under intensive GMP cleaning
Life Safety
Solves: Safe evacuation without destroying cleanroom pressure and layout logic
High Efficiency
Solves: Maintaining ISO Class 4-8 cleanroom environments
Ultra High Efficiency
Solves: Critical applications requiring ultra-low particle counts
Modular Air Supply
Solves: Flexible cleanroom ceiling layouts and retrofits
Fast Start
Solves: Flexible cleanroom ceiling layouts and retrofits and the 1st protection
Easy Upgrade
Solves: Flexible cleanroom ceiling layouts and retrofits
Max Performance
Solves: Superior contamination control in compact layouts
Heat Ready
Solves: Dependable cleanroom performance and retrofits where temperature is a critical factor
Pure Air
Solves: Achieving and maintaining highest air purity standards in adaptable ceiling layouts.
Differential Pressure During Transfer
Solves: Safe transfer of materials between different cleanliness zones
Zero Leakage
Solves: Safe transfer of materials between different cleanliness zones
Cycle Validated
Solves: High-level surface decontamination of materials entering sterile cores or isolators, reducing transfer time.
Comprehensive Sterilization
Solves: Provides validated, high-level sterilization gateway for a wide range of non-thermal tolerant materials entering aseptic areas
Particulate Scrubbing
Solves: Removes loose surface particulates from personnel garments before entry into critical zones
Surface Decontamination
Solves: Removing particles from personnel before entering clean zones
Mandatory Safety
Solves: Enforces mandatory personal decontamination for personnel exiting potent compound or high-containment areas, protecting the external environment and complying with strict health & safety protocols
Emergency Rinse
Solves: Provides immediate first-aid decontamination for accidental chemical exposure on personnel, minimizing injury severity and facilitating emergency response within labs or production areas
Localized Cleanliness
Solves: Creating localized clean environments for sensitive processes
Flexible Protection
Solves: Provides temporary, movable particle-free workspace for batch-specific tasks, spot repairs without the cost and lead time of fixed installation
Contained Dispensing
Solves: Safely contains high-potency powders during sampling, weighing, and dispensing operations, minimizing cross-contamination and operator exposure to hazardous active pharmaceutical ingredients (APIs)
Product Protection
Solves: Protects sensitive products or processes from ambient particulate contamination during assembly, packaging, or inspection tasks where operator protection is not the primary requirement
Safe Filter Change
Solves: Enables the safe removal and replacement of contaminated HEPA/ULPA filters in exhaust or intake systems, protecting maintenance personnel and the environment from hazardous particulates
Ergonomic Seating
Solves: Provides stable, non-shedding seating for gowned personnel during extended tasks, minimizing fatigue and particle generation without contamination or static risks.
Process Work Surfaces
Solves: Delivers a rigid, easy-to-sanitize foundation for critical processes (e.g., assembly, inspection, packaging)
Material Storage
Solves: Preserves the cleanliness and organization of in-process materials, tools, and components
Vertical Process Flow
Solves: Maximizes vertical space for organized, accessible staging of components during batch production
Vertical Process Flow
Solves: Enables safe, contained transfer of tools, samples, or instruments between zones without compromising cleanliness
Hygienic Point-of-Use
Solves: Provides a compliant, easy-to-sanitize hand hygiene station directly within the gowning or process area
Validated Purification
Solves: Reliably produces USP Purified Water from pretreated feed water by removing ions, organics, and microorganisms, ensuring consistent quality for pharmaceutical production and laboratory use
Thermal Assurance & Polishing Treatment
Solves: Consistent WFI production
that meets USP endotoxin and sterility assurance requirements without relying on chemical sanitization, suitable for parenteral and sterile product manufacturing.
PW/WFI Microbial Control & Loop Integrity
Solves: Maintaining produced water quality from generation through every point of use, day after day
Intrinsic Sterility
Solves: Providing sterile, non-pyrogenic steam suitable for direct product contact and critical sterilization processes
Precise Batching
Solves: Ensuring consistent, contamination-controlled preparation of pharmaceutical solutions prior to filling or processing
Aseptic Processing & Integrity
Solves: Enables the high-speed, aseptic filling of sterile liquids (vaccines, biologics, ophthalmics) without compromising sterility assurance, directly supporting compliance with Annex 1 and reducing product loss from contamination or fill variation.
Containment Certainty
Solves: Safe handling of potent or hazardous materials without compromising product quality or operator safety
Penetration Reliability
Solves: Achieving reliable sterilization of instruments, materials, and components prior to aseptic use
Uniform Lethality & Chemical-Free Sterilization
Solves: Reliable sterilization of heat-sensitive products and containers with reduced risk of cold spots or product damage
Seal Verification
Solves: Ensures the hermetic integrity of filled and sealed glass ampoules post-lyophilization, preventing sterility failure, moisture ingress, and product degradation throughout the shelf life
Inline Assurance
Solves: Performs reliable, non-destructive leak detection on single-piece plastic ampoules to guarantee container integrity for parenteral products, ensuring patient safety and compliance with regulatory standards for sterile packaging.
What types of cleanroom wall panels are available, and how do they differ in performance and application?
How do I choose between fire-rated panels and insulation-focused panels?
Are all panels suitable for different cleanroom iso classes?
Are hollow or honeycomb panels suitable for concealing utilities?
What is the difference between handmade and machine-made partition panels?