Clean Room Doors for Pharmaceutical Facilities: Key Considerations

Clean room doors play a critical role in maintaining the integrity of pharmaceutical facilities. These specialized doors are designed to ensure airtight sealing, contamination control, and easy accessibility while complying with stringent industry standards. The construction, material, and accessories used in clean room doors contribute to their efficiency, durability, and functionality.

Clean Room Doors: Features and Specifications

Clean room doors are manufactured with high-quality materials to ensure longevity and reliability. The double-skin door construction aligns with modular panels, providing seamless integration and enhanced performance.

Material and Construction

• Material of Construction: GPSP GI Sheet

  • Standard Thickness: 0.8mm (sheet), 1.2mm (frame)

  • Fire-Rated Doors: 1.2mm (sheet), 1.6mm (frame)

• Shutter Thickness: 42mm / 44mm / 46mm

• Paint/Finish: Powder-coated or Stainless Steel

• Powder Coating Thickness: 60-80 microns

Available Sizes

• Frame Thickness: 50mm, 80mm, 100mm, 150mm

• Door Width Options (mm): 750, 900, 1000, 1200, 1500, 1800, 2000, 2200

Accessories for Enhanced Functionality

• Hinges: 3-4 stainless steel hinges per door

• Handles: Stainless steel ‘D’ type handles (20mm diameter, 300mm long)

• Push Plate: Stainless steel (125mm x 300mm)

• Door Closure: Dorma TS-68 standard arm

• Locking Mechanism: Key-operated locking system on both sides

• Sealing System: Automatic door bottom seal

• View Panel: 6mm thick safety glass

• Emergency Exit: Equipped with a panic bar for quick access

• Double Door Features: Flush tower bolt for secure closure

• Protection Add-ons: Stainless steel kick plate (300mm height)

• Door Interlocking: Ensures restricted access and contamination control

Filler Material Options for Insulation

• PUF: 40±2 kg/m³

• PIR: 48±2 kg/m³

• ROCKWOOL: 96±2 kg/m³

Key Considerations for Pharmaceutical Clean Room Doors

1. Compliance with Industry Standards – Ensuring that the doors meet pharmaceutical safety and hygiene regulations.

2. Durability & Strength – Constructed from robust materials to withstand harsh environments.

3. Sealing Efficiency – Proper insulation and sealing mechanisms to prevent contamination.

4. Easy Maintenance & Cleaning – Smooth surfaces and high-quality finishes for easy upkeep.

5. Customization – Tailor-made door dimensions and accessories to fit specific project requirements.

Conclusion

Clean room doors are an essential component of pharmaceutical facilities, contributing to contamination control, safety, and efficiency. With high-quality materials, customizable specifications, and advanced sealing mechanisms, these doors provide a reliable solution for maintaining the integrity of controlled environments. Investing in well-constructed clean room doors ensures long-term performance and regulatory compliance.