About PPGI Clean Room
PPGI Clean Room is a room within which the number concentration of airborne particles is controlled and classified, and which is designed, constructed and operated in a manner to control the introduction, generation and retention of particles inside the room. PPGI Clean Room is made with a thin coating layer that consists of 18-20 microns, and continuous lines are used in the sheet manufacturing facility.
Product Type -PPGI Clean Room
Material - Galavanized Iron
Advanced Panel & Sealing TechnologyEngineered with PPGI panels finished in smooth, anti-static, and antimicrobial coatings, the system delivers superior hygiene and contamination control. The panel core options (PUF/EPS/Mineral Wool) are designed for durability and high sound insulation. Airtight silicone/polyurethane joint sealants support stringent cleanliness standards, while the modular design facilitates easy installation and future reconfiguration.
Comprehensive Compliance & SafetyEach cleanroom system complies with GMP, cGMP, ISO 14644, and FDA requirements. Panels meet fire-retardant norms established by IS and ASTM standards. Electrical fittings, HVAC with HEPA/ULPA filtration, and flush observation windows facilitate effective process monitoring and safety within pharmaceutical, medical, and high-tech manufacturing environments.
Customization & Versatile ApplicationPPGI Clean Rooms are available in a range of thicknesses, dimensions, and custom panel colors, suitable for diverse layouts and technical demands. Integrated features such as static/dynamic pass boxes with UV sterilization, walkable ceilings, modular partitions, and various flooring options ensure adaptability to unique project requirements.
FAQ's of PPGI Clean Room:
Q: How is the PPGI Modular Clean Room installed and customized for different layouts?
A: The clean room is constructed using modular PPGI panels that are manufactured to precise room dimensions as per client requirements. The panels, ceiling types, and other integrated accessories (such as pass boxes and observation windows) are customized to fit any specific room layout, ensuring rapid on-site installation and flexibility for future modifications.
Q: What are the main benefits of the anti-static and antimicrobial wall finish?
A: The anti-static and antimicrobial coating on the PPGI wall panels minimizes the accumulation of dust and prevents microbial growth. This feature is essential for environments where particulate and contamination control are critical, such as pharmaceutical and electronics manufacturing, leading to superior product quality and regulatory compliance.
Q: When should the cleanroom panels' insulation type (PUF, EPS, or Mineral Wool) be selected?
A: The panel insulation type should be chosen based on the required fire resistance, sound insulation, and thermal performance as dictated by your application. PUF offers high thermal insulation, Mineral Wool provides excellent fire resistance, and EPS is suitable for general insulation needs. Selection is typically done during project specification to match regulatory and process requirements.
Q: Where can PPGI Modular Clean Rooms be used?
A: These cleanrooms are widely used across the pharmaceutical, biotechnology, electronics, medical devices, and food processing industries in India. Their modularity and compliance with ISO, GMP, and FDA norms make them suitable for both new facility setups and facility upgrades.
Q: How is airtightness maintained in the cleanroom system?
A: Airtightness is ensured through the use of high-performance silicone or polyurethane sealants at panel joints, flush mounting of observation windows and electrical fittings, and properly sealed doors. This setup helps maintain positive air pressure and prevents contamination inflow or outflow, supporting ISO cleanroom classifications.
Q: What types of ceilings and floors are available for these cleanrooms?
A: You can choose between walkable and non-walkable ceiling panels based on maintenance needs. Flooring options include epoxy, ESD (Electrostatic Discharge), PVC, or antistatic vinyl, which can be selected according to process requirements and chemical resistance demands.
Q: What levels of cleanliness and filtration capabilities does the cleanroom offer?
A: The cleanroom supports Class 100 to 100,000 (ISO 5 to ISO 8) cleanliness levels. HEPA (99.97% at 0.3 micron) or ULPA filters are integrated into the HVAC system for effective air purification, ensuring that air quality remains consistent with pharmaceutical and high-tech industrial standards.