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Latest company case about HVAC System in Biopharmaceutical Cleanroom Engineering

HVAC System in Biopharmaceutical Cleanroom Engineering

Key Points of HVAC System Design and Construction 1. Sound-Absorbing Wall Panels in Air Conditioning Room The sound-absorbing wall panels in the air conditioning room are an important part of the HVAC system, mainly used to reduce noise generated by equipment operation. The panels typically use porous sound-absorbing materials such as fiberglass or rock wool, covered with perforated metal sheets or acoustic fabric to achieve optimal noise reduction. During installation, attention must be paid to the sealing of panel joints to ensure overall sound insulation performance. 2. Overall Effect of Air Conditioning Room The overall effect of the air conditioning room not only relates to aesthetics but also directly affects equipment efficiency and maintenance convenience. The design should consider rational equipment layout to ensure smooth airflow organization while reserving sufficient space for maintenance. Walls and ceilings in the room are usually made of cleanroom-compatible panels, and the floor is made of anti-static, wear-resistant materials. Light colors are preferred for easy detection of dust and stains. 3. Color-Coded Insulation in Air Conditioning Room Pipes and equipment in the air conditioning room require insulation to minimize energy loss and prevent condensation. Color-coded insulation materials not only provide excellent thermal insulation but also help distinguish different pipeline systems (e.g., chilled water, hot water, steam) for easy identification and maintenance. A protective layer is usually added over the insulation to prevent mechanical damage and extend service life. 4. Installation of Outer Protective Panels Outer protective panels are essential for shielding the insulation layer and enhancing the appearance of pipelines. During installation, attention must be paid to panel alignment and fastening methods to ensure a smooth and visually appealing finish. For cleanroom areas, the outer panels should be made of low-particulate, easy-to-clean materials, with sealed joints. Additionally, the color and labeling of the panels must comply with relevant standards and client requirements.  
2025-06-16
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Latest company case about Unveiling the

Unveiling the "Cleaning Guardian" in Biopharmaceuticals: The Working Mysteries and Application Value of Fog Shower Chambers

——Guangzhou Cleanroom Construction Co., Ltd. Leads You to Explore the Clean Technology in Biopharmaceuticals​ In the "microscopic battlefield" of biopharmaceuticals, even a single dust particle or microorganism can be an "invisible killer" threatening the quality of drugs. To safeguard drug safety, the industry has extremely stringent requirements for the cleanliness of the production environment. Among the numerous devices ensuring a clean environment, the fog shower chamber acts like a meticulous "cleaning guardian," building a crucial defense line for drug production with its fine mist curtain. As Guangzhou Cleanroom Construction Co., Ltd., which has deep - rooted experience in the purification equipment field, let's take an in - depth look at this important device in the biopharmaceutical industry.​   Why is the Fog Shower Chamber Indispensable in Biopharmaceuticals?——The Imperative Need for Clean Production​   During the biopharmaceutical process, due to the specificity of drug ingredients and the complexity of production processes, the requirements for environmental cleanliness are extremely high. Once contaminants such as microorganisms and dust mix in, it will not only lead to drug deterioration and loss of efficacy but may also trigger serious medical accidents. For example, in vaccine production, even a tiny amount of bacterial contamination can render the vaccine ineffective and even endanger the health of vaccine recipients.​ Strict domestic and international regulations also clearly define the cleanliness standards for biopharmaceuticals. The cGMP of the US FDA, the GMP of the European Union, and China's "Good Manufacturing Practice for Drugs" all set strict regulations on indicators such as the number of suspended particles and microbial content in production workshops. Take Class A clean areas as an example, the number of particles ≥ 0.5μm per cubic meter of air should not exceed 3,520, and the number of microbial colonies should approach zero. Under such high - standards, the fog shower chamber has become an indispensable device for ensuring clean production.​   How Does the Fog Shower Chamber Work?——The "Cleaning Magic" of Precise Design​   1. A Complete Analysis of the Working Process When personnel or materials enter the fog shower chamber, the sensing device is immediately activated. The fan sucks in ambient air, which is filtered through primary, medium - efficiency, and high - efficiency filters to ensure that the air entering the fog shower chamber reaches a high level of cleanliness. At the same time, the atomization system atomizes clean water into micron - sized mist drops, forming a fine mist curtain. These mist drops quickly capture dust, microorganisms, and other contaminants adhering to the surface of personnel or materials, causing them to settle to the ground and finally be discharged through the drainage system. The entire process can complete efficient purification in just tens of seconds.​ 2. Highlights of Core Technologies​ Micron - level Atomization Technology: Ultrasonic or pressure atomizers are used to atomize water into mist drops of 5 - 10 microns, greatly increasing the contact area between the mist drops and contaminants and improving the purification efficiency.​ Multi - stage Filtration System: The primary filter intercepts large - particle dust; the medium - efficiency filter further filters smaller particles; the high - efficiency filter (with a filtration efficiency of 99.97%@0.3μm) ensures that the air entering the fog shower chamber meets the cleanliness standard.​ Intelligent Control System: It can achieve functions such as automatic induction activation, mist volume adjustment, and operation time setting. It can also monitor parameters such as temperature, humidity, and pressure in the fog shower chamber in real - time to ensure stable operation of the equipment.​ The Unique Advantages of the Fog Shower Chamber——Superiority Shown in Comparison​ ​ Comparison Items​ Traditional Air Shower Chamber​ Fog Shower Chamber​ Purification Principle​ Blowing away contaminants with high - speed airflow​ Adsorbing and settling contaminants with mist drops​ Purification Effect​ Limited purification effect on tiny particles and microorganisms​ Can effectively remove micron - sized particles and microorganisms, with a higher purification rate​ Applicable Objects​ Mainly for personnel​ Applicable to personnel, materials, and equipment​ Energy Consumption​ High energy consumption due to long - term high - speed operation of the fan​ Relatively low energy consumption​ Noise Performance​ High noise during fan operation​ Low operating noise, creating a quieter working environment​ ​ Application Scenarios of the Fog Shower Chamber in Biopharmaceuticals——Ubiquitous Protection​   1. Personnel Purification​ Before entering the sterile production area, staff members must pass through the fog shower chamber. The fine mist curtain can quickly remove dust, dander, and microorganisms on the surface of clothing, preventing contaminants from being brought into the workshop. For example, in an insulin production workshop, staff members enter and exit the fog shower chamber multiple times a day to ensure they are in a clean state.​ 2. Material Purification​ Raw materials, packaging materials, etc. also need to be purified through the fog shower chamber before entering the production area. For example, after passing through the fog shower chamber, tiny particulate contaminants on the surface of pharmaceutical glass bottles are effectively removed, avoiding affecting the quality of drugs.​ 3. Equipment Cleaning​   Production equipment is regularly cleaned through the fog shower chamber, which can reduce the residue of contaminants on the equipment surface, ensure the normal operation of the equipment, and reduce the risk of the equipment polluting the production environment.​   The Fog Shower Chambers of Guangzhou Cleanroom Construction Co., Ltd.——The Combination of Quality and Innovation​   As a professional purification equipment supplier, the fog shower chambers of Guangzhou Cleanroom Construction Co., Ltd. are highly favored in the biopharmaceutical industry due to their advanced technology and reliable quality. Our fog shower chambers are made of food - grade 304 stainless steel, which is corrosion - resistant and easy to clean. The optimized air duct system ensures a more uniform distribution of mist drops and a more stable purification effect. We can also provide personalized customization services according to customer needs to meet the requirements of biopharmaceutical enterprises of different scales and processes.​   From a single dust particle to a bottle of good medicine, every link embodies the power of technology. The fog shower chamber, the "cleaning guardian" of the biopharmaceutical industry, protects the cleanliness of the drug production environment with precision and efficiency. In the future, Guangzhou Cleanroom Construction Co., Ltd. will continue to deepen its exploration in the purification field and escort the high - quality development of the biopharmaceutical industry with innovative technologies.
2025-06-16
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Latest company case about High-Efficiency Exhaust Air Outlets in Biopharmaceuticals: Key Equipment for Ensuring Clean Production Environments

High-Efficiency Exhaust Air Outlets in Biopharmaceuticals: Key Equipment for Ensuring Clean Production Environments

——Product Analysis of High-Efficiency Exhaust Air Outlets by Guangzhou Cleanroom Construction Co., Ltd.   In the highly precise and environmentally demanding biopharmaceutical industry, every production process is crucial for the quality, safety, and effectiveness of drugs. Among these, maintaining the cleanliness of the production environment is of utmost importance, and high-efficiency exhaust air outlets play an irreplaceable role in this process. As Guangzhou Cleanroom Construction Co., Ltd., with years of in - depth experience in the purification equipment field, we have a profound understanding of the needs of the biopharmaceutical industry and are committed to providing customers with excellent high-efficiency exhaust air outlet products and solutions. Stringent Requirements for Exhaust Air in Biopharmaceutical Production Environments During biopharmaceutical production, various pollutants are generated, including microorganisms, harmful dust, chemical gases, and biological aerosols. If these pollutants are not promptly and effectively removed from the production area, they will accumulate continuously in the workshop, seriously threatening the quality of drugs. For example, the growth of microorganisms may contaminate drugs, leading to drug deterioration, loss of efficacy, and even posing a serious threat to patients' health. Harmful dust and chemical gases not only affect the normal operation of production equipment, shortening its service life, but may also react chemically with drugs, altering their composition and properties.   At the same time, the biopharmaceutical industry is subject to numerous strict regulations and standards, such as China's "Good Manufacturing Practice for Drugs" (GMP), the relevant regulations of the US Food and Drug Administration (FDA), and the European Union's "Current Good Manufacturing Practice" (cGMP). These regulations and standards put forward extremely specific and strict requirements for the air quality of the production environment and the performance of the exhaust air system. Taking GMP as an example, it clearly stipulates the limits for airborne particles and microbial content in production areas of different cleanliness levels, as well as key indicators such as the filtration efficiency and airtightness of the exhaust air system, ensuring that the drug production process is always in a controlled environment that meets quality standards. Technical Advantages of High-Efficiency Exhaust Air Outlets by Guangzhou Cleanroom Construction Co., Ltd. Advantage Dimension Technical Features Practical Utility Superior Filtration Performance Equipped with top - grade high-efficiency filters with a filtration efficiency of up to 99.97% (for particles with a particle size of 0.3μm), and the filter design is optimized to increase the filtration area. Precisely intercept tiny particulate pollutants, extend the service life of the filter, reduce maintenance costs, and ensure a clean workshop environment. Excellent Airtight Design The casing of the exhaust air outlet is manufactured by seamless full - welding technology, and the welds are strictly inspected by flaw detection. High-performance sealing materials and advanced sealing structures are used at all connection points, with a leakage rate of less than 0.1% under a pressure of 1Kpa. Prevent the leakage of unfiltered polluted air, avoid the spillage of pollutants in the workshop, and ensure the safety of the surrounding environment and personnel. Convenient In-situ Disinfection and Leak Detection Functions Special disinfection interfaces are reserved, which can be conveniently connected to external disinfection equipment such as hydrogen peroxide disinfectors. An advanced in-situ automatic scanning leak detection device is equipped to conduct real-time scanning detection of the filter, accurately locate the leak point and issue an alarm once a leakage problem is found. Ensure that the interior of the equipment is sterile, promptly detect and handle filter leakage problems, and improve the reliability and safety of equipment operation. Structural Design and Material Selection of the Product Design Dimension Design/Material Key Points Application Advantages Reasonable Structural Design Compact structure, small space occupation; optimized air inlet guide structure, and the air outlet ensures cleanliness; the maintenance door is easy to open. Facilitates installation and maintenance in the workshop, improves filtration efficiency, avoids secondary pollution, and shortens equipment downtime. High-Quality Material Selection The casing and key components are made of high-quality stainless steel, and non-toxic and odorless materials that meet food and drug safety standards are used for parts in direct contact with air. Corrosion-resistant, high-strength, easy to clean, adaptable to complex environments, and ensures the safety of the drug production environment. Conclusion The high-efficiency exhaust air outlets of Guangzhou Cleanroom Construction Co., Ltd., with their excellent technical performance, reasonable structural design, and high-quality material selection, have become a reliable choice for ensuring the cleanliness of production environments in the biopharmaceutical industry. We always adhere to the attitude of striving for excellence, continuously innovate and optimize our products, and are committed to providing customers with the highest quality products and services. If you have any needs for the construction or renovation of exhaust air systems in biopharmaceutical workshops, please feel free to contact us. We will wholeheartedly provide you with professional solutions to help your enterprise move forward steadily in the biopharmaceutical field.  
2025-06-16
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Latest company case about Guangzhou Cleanroom Construction Co., Ltd.: The Premier Creator of Laboratory Engineering

Guangzhou Cleanroom Construction Co., Ltd.: The Premier Creator of Laboratory Engineering

Opening the virtual "door to the laboratory," one is greeted with a spectacular showcase where technology and craftsmanship converge. As a leading provider of laboratory engineering solutions, Guangzhou Cleanroom Construction Co., Ltd. leverages its profound technical expertise and innovative design concepts to meticulously craft laboratory projects that seamlessly integrate functionality, safety, and comfort. From the efficient collaboration in comprehensive offices to the rigorous exploration in precision laboratories, every space reflects our professionalism and quality. Now, let’s take an in - depth look at these stunning renderings of our laboratory engineering projects. I. Comprehensive Office: Open Collaboration, Smart Workspace Spatial Layout The comprehensive office features an open - plan layout, with smooth circulation lines that break down spatial barriers. Light - colored modern office furniture complements the panoramic floor - to - ceiling windows, allowing natural light to flood the space and creating a transparent, comfortable working atmosphere for employees. Intelligent Facilities Smart meeting screens, high - speed network interfaces, and other facilities are ingeniously integrated, meeting the needs of team brainstorming and remote collaboration. Flexible partition devices can not only ensure private office scenarios but also be switched to an open communication mode at any time, achieving a perfect balance between efficiency and focus. II. R&D Laboratory: Cutting - Edge Technology, the Cornerstone of Exploration Experimental Bench Configuration In the renderings of the R&D laboratory, modular experimental benches are neatly arranged, equipped with intelligent water and electricity control systems and negative pressure ventilation devices, eliminating experimental risks from the source. Functional Zoning The central operation area, precision instrument area, and sample storage area are strictly separated, ensuring the scientific and standardized experimental process. Environmental Control The anti - glare shadowless lighting system and constant temperature and humidity control create a stable and precise experimental environment for researchers. Reserved expansion spaces and standardized interfaces endow the laboratory with the flexibility to upgrade and adapt to future research needs. III. Reagent Room: Safety Assurance, Standardized Storage Safety Facilities Safety is the top priority in the renderings of the reagent room. Explosion - proof reagent cabinets with dual - lock control and intelligent temperature - sensing monitoring make the storage status of hazardous chemicals visible in real - time. Fire - proof and explosion - proof walls, together with independent exhaust systems, form multiple protective barriers. Storage Management Reagents are color - coded and classified according to their chemical properties and hazard levels. Paired with electronic tags and an inventory management system, quick and accurate access is achieved. A 24 - hour gas leakage monitoring device constantly safeguards the safety of the laboratory. IV. Physical and Chemical Laboratory: Precision and Rigor, Quality Assurance Equipment and Benches Focusing on high - precision experimental requirements, the Physical and Chemical Laboratory is equipped with customized shock - proof experimental benches carrying high - precision balances, spectrometers, and other equipment, effectively isolating external vibration interference. Environmental Maintenance The special anti - static and anti - corrosion floor treatment extends the service life of the equipment. The intelligent temperature and humidity control system and fresh air filtration device ensure a stable and controllable experimental environment. Lighting Design The adjustable lighting system meets the lighting requirements of different experimental scenarios, assisting researchers in obtaining more accurate experimental data. V. Conference Room: Efficient Communication, the Decision - making Hub Meeting Equipment The conference room adopts an immersive design. A circular conference table, combined with high - definition touch - control large screens, supports wireless screen mirroring and real - time annotation of multiple devices, making information sharing more intuitive. Environmental Creation Sound - absorbing wall panels and double - layer sound - insulation glass isolate external noise, creating a quiet discussion space. Video conferencing systems, intelligent sound reinforcement equipment, etc., are all available, enabling efficient communication for both remote collaboration and internal discussions, providing solid support for scientific research decision - making. VI. Factory Director's Office: Grand and Stable, Strategic Command Center Space Planning The Factory Director's Office presents a stable and grand style, with a reasonable layout of independent reception areas, office areas, and rest areas. Panoramic floor - to - ceiling windows offer a broad view of the entire laboratory park, creating an open perspective. Equipment and Security Solid wood office furniture, combined with intelligent office equipment, demonstrates the professionalism and taste of management. Intelligent access control and document encryption systems ensure the security of core decision - making information, creating a private and efficient management space. VII. Packaging Material Room: Efficient Circulation, Orderly Management Warehousing Design The Packaging Material Room adopts a three - dimensional warehousing design. High - level shelves, combined with intelligent forklift systems, greatly improve space utilization. RFID electronic tags are linked with the inventory management software to achieve automated registration and precise positioning of packaging materials during inbound and outbound processes. Quality Inspection and Transportation A dedicated quality inspection area is equipped with professional testing equipment to ensure that every piece of packaging material meets high - standard requirements. The spacious passage planning ensures the efficient transportation of materials. VIII. Microbiology Laboratory: Ultimate Cleanliness, a Sterile Paradise Purification System The Microbiology Laboratory is designed in strict accordance with cleanroom standards, equipped with a laminar flow purification system that filters dust particles and microorganisms in the air to a class 100 cleanliness level. Anti - bacterial Design The walls and floors are seamlessly connected and coated with antibacterial materials, facilitating thorough disinfection. Independent buffer rooms, changing areas, and transfer windows form a complete contamination isolation chain, preventing external interference. Environmental Monitoring The intelligent environmental monitoring system provides real - time feedback on data such as temperature, humidity, and pressure difference, providing a sterile and stable ideal environment for microbiological experiments.   Guangzhou Cleanroom Construction Co., Ltd. has always been customer - oriented. From space planning and equipment configuration to detailed craftsmanship, every aspect reflects our dedication. These renderings of laboratory engineering projects are not only visual presentations but also epitomize the company's technical strength and service quality. In the future, we will continue to deepen our commitment to the laboratory engineering field, drive development through innovation, create more high - quality and professional laboratory spaces for scientific research, and assist our clients in reaching new heights of scientific exploration.
2025-06-13
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Latest company case about Process Water Supply in Biopharmaceutical Cleanroom Engineering

Process Water Supply in Biopharmaceutical Cleanroom Engineering

1. Pump Equipment Grounding Pump equipment grounding is a critical aspect of ensuring the safe operation of the process water supply system. Grounding must comply with electrical safety standards to prevent static buildup and leakage risks, and regular testing of grounding resistance values is required. 2. Valve Group Installation Valve group installation must strictly follow the process flow diagram to ensure correct valve type, direction, and positioning. After installation, leak testing must be performed to prevent leakage, and the valve status should be clearly marked for operation and maintenance. 3. Clear and Aesthetic Pipeline Labeling Pipeline labels should include information such as medium name, flow direction arrows, and pressure ratings, using a standardized label format. Labels must be clear, visible, and securely attached to avoid detachment or fading. 4. Finished Wall Sleeve Installation Wall sleeve installation requires proper gap allowance, filled with sealing material to ensure the airtightness of the cleanroom. The sleeve material should match the pipeline, and after installation, sealing performance must be checked with appropriate anti-corrosion treatment applied.  
2025-06-13
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Latest company case about Cleanroom Enclosure Structure in Biopharmaceutical Cleanroom Engineering

Cleanroom Enclosure Structure in Biopharmaceutical Cleanroom Engineering

Design and Construction Key Points of Cleanroom Enclosure 1. Uniform Layout of CNC Corridor The layout design of CNC corridors must strictly adhere to cleanroom engineering standards, ensuring all components are arranged uniformly. Seams between walls, ceilings, and floors should be seamless to prevent dust accumulation. Materials should be corrosion-resistant and easy to clean, such as stainless steel or specially coated panels. The layout must account for equipment pipeline routing, reserve access panels, and maintain visual neatness. 2. Installation of CNC Corridor During CNC corridor installation, the flatness and verticality of the base structure must meet requirements. The installation sequence should follow the principle of working from the inside out and top to bottom. All connection points must be sealed with specialized sealant to ensure airtightness. After installation, cleanliness testing must be conducted to verify compliance with the required ISO classification standards. 3. Installation of Floor-to-Ceiling Windows Floor-to-ceiling windows in clean areas should use double or triple-pane tempered glass filled with inert gas for improved insulation and soundproofing. Window frames should be made of aluminum alloy or stainless steel with anodized surfaces. Special attention must be paid to sealing the joints between window frames and walls using structural silicone sealant to ensure airtightness. Glass surfaces should be coated with anti-static film to prevent dust adhesion. 4. Installation of External Windows External windows must meet basic airtight and waterproof requirements while also addressing the special needs of clean areas. Window sashes should be fixed or non-operable to minimize external contamination. Laminated safety glass with UV-filtering interlayers is recommended. Continuous waterproof and vapor barriers must be installed at the junctions between window frames and walls, along with thermal insulation to prevent thermal bridging.
2025-06-13
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Latest company case about Drainage System Components in Biopharmaceutical Cleanroom Engineering

Drainage System Components in Biopharmaceutical Cleanroom Engineering

Critical Elements of Pharmaceutical Grade Drainage Systems The drainage system in biopharmaceutical cleanroom engineering is a critical component that ensures compliance with GMP (Good Manufacturing Practice) requirements. The system must meet stringent hygiene standards, contamination control specifications, and fluid management regulations. 1. Aesthetic Welding of Drainage Risers Drainage riser welds must meet the following requirements: Automatic welding processes to ensure uniform and smooth welds (per ASME BPE-2019 standard) Weld surface roughness Ra≤0.5μm (ISO 1302 standard) 100% endoscopic inspection (ASTM E1417 standard compliant) 2. Installation of Drain Pipe Traps Trap installations must comply with: Item Requirement Standard Reference Water Seal Depth ≥50mm GB 50015-2019 Material 316L Stainless Steel ASME BPE-2019 Cleaning Method CIP/SIP Compatible ISPE Baseline Guide 3. Rational and Aesthetic Layout of Process Equipment Drainage Equipment drainage layout principles: Gravity drainage design with ≥1% slope (FDA cGMP compliant) Drain point-to-equipment distance ≤1.5m (ISPE recommended value) ·Sanitary clamp connections (3A Sanitary Standard) 4. Equipment Wiring Conduits Wiring conduit installation requirements: IP68 protection rating (IEC 60529 standard) ·316 stainless steel material (ASTM A276 standard) 5° anti-pooling tilt design (PIC/S PI 007 recommendation)  
2025-06-12
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Latest company case about Drainage System Components in Biopharmaceutical Cleanroom Engineering

Drainage System Components in Biopharmaceutical Cleanroom Engineering

Critical Elements of Pharmaceutical Grade Drainage Systems The drainage system in biopharmaceutical cleanroom engineering is a critical component that ensures compliance with GMP (Good Manufacturing Practice) requirements. The system must meet stringent hygiene standards, contamination control specifications, and fluid management regulations. 1. Aesthetic Welding of Drainage Risers Drainage riser welds must meet the following requirements: Automatic welding processes to ensure uniform and smooth welds (per ASME BPE-2019 standard) Weld surface roughness Ra≤0.5μm (ISO 1302 standard) 100% endoscopic inspection (ASTM E1417 standard compliant) 2. Installation of Drain Pipe Traps Trap installations must comply with: Item Requirement Standard Reference Water Seal Depth ≥50mm GB 50015-2019 Material 316L Stainless Steel ASME BPE-2019 Cleaning Method CIP/SIP Compatible ISPE Baseline Guide 3. Rational and Aesthetic Layout of Process Equipment Drainage Equipment drainage layout principles: Gravity drainage design with ≥1% slope (FDA cGMP compliant) Drain point-to-equipment distance ≤1.5m (ISPE recommended value) ·Sanitary clamp connections (3A Sanitary Standard) 4. Equipment Wiring Conduits Wiring conduit installation requirements: IP68 protection rating (IEC 60529 standard) ·316 stainless steel material (ASTM A276 standard) 5° anti-pooling tilt design (PIC/S PI 007 recommendation)  
2025-06-12
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Latest company case about Electrical Systems in Biopharmaceutical Cleanroom Engineering

Electrical Systems in Biopharmaceutical Cleanroom Engineering

Power Distribution System Design and Installation Specifications 1. Distribution Cabinet Wiring Distribution cabinet wiring is a critical component of biopharmaceutical cleanroom electrical systems and must comply with IEC 60439-1 "Low-voltage switchgear and controlgear assemblies". Key considerations include: 1. Use specialized crimping tools to ensure proper terminal-to-conductor contact 2. Conductor cross-sections must meet load requirements per NEC 310.15 3. Stranded wires must use crimped terminals to prevent fraying 4. Clear phase identification per IEC 60446 color standards 2. Cable Installation Cleanroom area cable installation must meet FDA cGMP and ISO 14644 standards: 1. Cable trays should be 304 stainless steel with smooth, burr-free surfaces 2. Segregation of power and control cables with ≥300mm spacing (per IEC 60364-5-52) 3. Use sealed conduits when penetrating cleanroom walls to maintain pressure balance 4. All cables must have flame-retardant properties meeting UL 94 V-0 3. Conduit Installation Special requirements for cleanroom conduit installation: 1. Use 316L stainless steel seamless tubes with internal surface roughness Ra≤0.8μm 2. Minimum bending radius ≥6× conduit diameter (ASME BPE-2016 standard) 3. Support spacing ≤1.5m with non-shedding fasteners 4. Ground continuity test resistance ≤0.1Ω (IEC 60664-1) 4. Distribution Cabinet Installation Cleanroom distribution cabinet installation standards: 1. Mount ≥300mm above floor to prevent contamination (GMP Annex 1) 2. Enclosure protection rating ≥IP54 (IEC 60529) 3. Positive pressure design with ≥5Pa differential (ISO 14644-3) 4. Emergency disconnect devices per IEC 60947-3 Relevant International Standards: • ISO 14644 Cleanrooms and associated controlled environments • IEC 60364 Low-voltage electrical installations • ASME BPE Bioprocessing Equipment Standard • EU GMP Annex 1 Manufacture of Sterile Medicinal Products • NFPA 70 National Electrical Code (USA)
2025-06-12
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Latest company case about Air Shower Pass Box: Unpacking and Inspection Guide for Safe and Proper Use

Air Shower Pass Box: Unpacking and Inspection Guide for Safe and Proper Use

The Air Shower Pass Box (also known as a Cleanroom Pass-Through) is a critical device used in controlled environments such as pharmaceutical labs, electronics manufacturing, and biotechnology facilities. It ensures contamination-free transfer of materials between different cleanroom zones. To guarantee optimal performance and safety, proper unpacking, inspection, and initial setup are essential. This guide provides step-by-step instructions for handling your new Air Shower Pass Box while emphasizing safety precautions. 1. Safe Unpacking Procedures ① Pre-Unpacking Preparation l Ensure the unpacking area is clean and dry to prevent contamination or moisture damage. l Use gloves and proper tools (e.g., a box cutter or scissors) to avoid damaging the unit. l Inspect the outer packaging for signs of severe impact, water damage, or mishandling. ② Step-by-Step Unpacking l Carefully remove the outer packaging—avoid using excessive force. l Check the shipping documents to confirm the model matches your order. l Lift the unit with two people (if heavy) to prevent accidental drops. l Verify all accessories against the packing list (e.g., power cables, filters, manuals). ⚠ If any damage or missing parts are found, DO NOT proceed—contact the supplier immediately. 2. Initial Inspection Checklist ① Visual Inspection ✔ Exterior: No dents, scratches, or deformities on stainless steel surfaces.✔ Doors & Seals: Smooth operation, no air leaks.✔
2025-06-30
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Latest company case about Mechanical Interlocking Air Shower Pass Box – SUS304 Stainless Steel with UV Sterilization

Mechanical Interlocking Air Shower Pass Box – SUS304 Stainless Steel with UV Sterilization

In cleanrooms, pharmaceutical facilities, and electronics manufacturing, maintaining contamination control during material transfer is critical. The Mechanical Interlocking Air Shower Pass Box provides a secure, efficient solution by combining particle removal and UV sterilization in one system. Product Highlights l Full SUS304 stainless steel construction – Corrosion-resistant, durable, and easy to sanitize l Built-in air shower system – HEPA-filtered high-velocity airflow removes surface particles l UV sterilization lamp – Eliminates microorganisms for aseptic transfers l Single-pane tempered glass door – 5mm safety glass with clear visibility l Rounded internal corners – Smooth radius design prevents particle accumulation l Dual-door mechanical interlock – Ensures only one door opens at a time to maintain pressure differentials Key Components l Illumination switch – Controls interior LED lighting l Stainless steel handle – Ergonomic design with smooth operation l 5mm tempered viewing window – Maintains visibility while containing airflow l Power connection port – Standard IEC inlet with emergency cutoff l Germicidal UV-C lamp – 254nm wavelength for 99% microorganism kill rate Technical Specifications l External dimensions: 500(W)×500(H)×500(D)mm l Internal workspace: 330(W)×430(H)×330(D)mm l Air velocity: 20-25 m/s (adjustable) l HEPA filtration: 99.99% @ 0.3μm Industry Applications ✔ Pharmaceutical manufacturing✔ Microelectronics cleanrooms✔ Biomedical research labs✔ Food processing ISO Class 5-8 environments This system meets ISO 14644-1 and GMP Grade B requirements for particulate control. The integrated air shower and UV sterilization provide dual protection against both airborne and surface contaminants. Customization Options Available: l Additional HEPA banks for higher cleanliness levels l RFID access control systems l Pressure monitoring gauges l VHP (vaporized hydrogen peroxide) compatibility For specific cleanroom validation requirements or technical drawings, please contact our engineering team.  
2025-06-27
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Latest company case about Transportation and Storage Guidelines for Air Shower Pass Box

Transportation and Storage Guidelines for Air Shower Pass Box

The Air Shower Pass Box (also known as a Cleanroom Pass-Through) is a critical component in maintaining contamination control in cleanroom environments. Proper transportation and storage are essential to ensure its performance and longevity. Below are the key guidelines to follow: 1. Transportation Guidelines The Air Shower Pass Box can be transported using standard methods (e.g., trucks, ships, or trains), but the following precautions must be taken: Protect from Rain & Snow – The equipment must be shielded from moisture to prevent rust, corrosion, or electrical damage. Secure Properly – Ensure the unit is firmly fixed during transit to avoid vibrations, impacts, or structural deformation. Handle with Care – Avoid rough handling during loading/unloading to prevent damage to sensitive components. 2. Storage Conditions To maintain the integrity of the Air Shower Pass Box, storage conditions must meet the following requirements: Temperature Range: -10°C to 40°C – Extreme temperatures can affect material integrity. Humidity Control: Relative humidity ≤80% – High humidity may cause rust or electrical malfunctions. No Corrosive Gases – Storage areas must be free from acidic, alkaline, or other corrosive chemicals. 3. Storage Duration The maximum storage period in its original packaging should not exceed 180 days. For long-term storage, inspect the unit periodically to ensure packaging remains intact and environmental conditions are stable. Conclusion Proper transportation and storage of the Air Shower Pass Box are crucial to maintaining its functionality and extending its service life. Before installation, conduct a thorough inspection to verify that all components are undamaged and ready for use. For further technical support, consult the manufacturer or supplier for detailed instructions!
2025-06-27
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Latest company case about Here Comes the “Guardian” of Flammable and Hazardous Chemicals!​

Here Comes the “Guardian” of Flammable and Hazardous Chemicals!​

When ordinary storage cabinets are “vulnerable” in the face of hazardous chemicals and traditional locks struggle to resist unauthorized access, Guangzhou Cleanroom Construction Co., Ltd. presents the explosion-proof cabinet with the dimensions of 900×450×1800mm, redefining the safety standards for hazardous chemicals storage with its outstanding strength!​ Steel Body, Indestructible​ Military-grade Material: The full-steel structure frame is integrally formed with 1.0mm thick cold-rolled steel plates, just like putting an “explosion-proof armor” on hazardous chemicals. Compared with ordinary cabinets, it can withstand more than 10 times the impact force. Even in case of severe collisions or high-temperature exposure, it remains rock-solid!​ Precision Craftsmanship: With seamless welding technology and double anti-rust coatings, it is moisture-proof, corrosion-resistant, and deformation-resistant. Whether in the humid south or high-temperature workshops, it can continuously safeguard the safety of hazardous chemicals.​ Intelligent Ventilation, Fresh Environment​ The built-in intelligent ventilation system is like installing a “respiratory system” for the explosion-proof cabinet:​ It monitors the gas concentration inside the cabinet in real time and automatically starts ventilation when the concentration exceeds the standard, quickly exhausting flammable and explosive gases;​ It features a silent design, ensuring no interference with the working environment;​ It supports both manual and automatic mode switching, flexibly adapting to different scenarios.​ Fingerprint Lock Control, Enhanced Security​ Say goodbye to the troubles of traditional keys, which are easy to lose or duplicate. The biometric fingerprint lock makes a powerful debut:​ It achieves ultra-fast identification in 0.3 seconds, precisely rejecting “unauthorized access”;​ It supports the entry of 100 sets of fingerprints, enabling hierarchical management of multiple users' permissions;​ With an emergency backup key, it provides dual protection for foolproof security.​ Optimal Dimensions, Space Master​ The scientific dimensions of 900×450×1800mm bring three major advantages:​ ✅ Occupying less than 0.5 square meters, it can be easily installed even in narrow spaces;​ ✅ With 3 adjustable shelves, it allows for free combination, ensuring that hazardous chemicals of all sizes have their proper place;​ ✅ There are pre - reserved wiring holes at the top, enabling easy connection to monitoring and alarm devices.​ The explosion-proof cabinets of Guangzhou Cleanroom Construction Co., Ltd. are not just storage tools but also a commitment to safety! From laboratories to chemical plants, from research institutions to production workshops, every place where hazardous chemicals are stored deserves such a “safety guard”!​   Contact Us to Customize Your Exclusive Explosion-proof Storage Solution and Make Safety “Visible and Tangible”!​Welcome to visit us for an up-close experience of the performance of the explosion-proof cabinet. We provide one-on-one solution design services!
2025-06-27
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Latest company case about A Comprehensive Analysis of Singapore's ISO 22000

A Comprehensive Analysis of Singapore's ISO 22000 "Food Safety Management System"

I. Introduction In the context of increasingly frequent global food trade, food safety has become a core issue concerning public health and industry development. As a crucial hub of international food trade, Singapore's rigorous implementation of the ISO 22000 "Food Safety Management System" has set a benchmark for global food safety management. Guangzhou Cleanroom Construction Co., Ltd., with its deep - rooted expertise in food workshop purification, has become a key partner for numerous enterprises in implementing the ISO 22000 standard and ensuring food safety, through its professional equipment and technologies. II. Synergy between the Core Contents of ISO 22000 and the Equipment of Guangzhou Cleanroom Construction Co., Ltd. (I) Deep Integration of the HACCP System ISO 22000 takes the HACCP system as its core. Singaporean food enterprises identify critical control points through a full - process hazard analysis. For example, a large - scale baking enterprise strictly detects pathogenic bacteria and agricultural residues during the raw material acceptance process, and precisely controls temperature and time during the baking stage. The air purification equipment of Guangzhou Cleanroom Construction Co., Ltd. adopts high - efficiency filtration technology, and its relevant performance data are shown in the following table:   Test Items Test Standards Test Results of Equipment from Guangzhou Cleanroom Construction Co., Ltd. Interception rate of 0.3 - micron particles ≥99.97% 99.99% Air cleanliness class Class A specified by ISO 22000 Meets Class A standard Bacterial filtration efficiency ≥99% 98%   This equipment creates a sterile barrier for food production, ensuring the effective implementation of the HACCP system. (II) Construction of an Intelligent Communication Mechanism The food safety information sharing platform established in Singapore enables data interconnection across the entire industry chain. Meanwhile, the real - time feedback of production environment data is equally crucial. The purification equipment of Guangzhou Cleanroom Construction Co., Ltd. is equipped with an IoT monitoring system, which can automatically collect 12 indicators such as workshop temperature, humidity, and dust particle count. Abnormal data can be pushed to managers' mobile phones within one second. After its application in a sauce processing factory, the system's early warning helped deal with filter blockage of the equipment in a timely manner, avoiding product contamination caused by poor air quality. The equipment failure response time has been significantly shortened, as shown in the following table:   Indicators Before Application After Application Average failure response time 48 hours 2 hours Unqualified product rate due to air quality issues 8% 1% (III) Support for Systematic Management Singaporean food enterprises incorporate food safety into their overall strategies, forming a closed - loop management from procurement to sales. Guangzhou Cleanroom Construction Co., Ltd. provides customized solutions. The adaptation of its equipment to different types of food processing scenarios is shown in the following table:   Food Processing Types Suitable Equipment Achieved Effects Meat processing Negative pressure purification workshop Effectively isolates odors and microorganisms, reducing the total number of colonies by 85% Beverage production Laminar flow hood Ensures a Class 100 clean environment for the filling process, increasing the product qualification rate to 99.5% Baked goods production Combined purification unit Stably controls temperature, humidity, and air cleanliness, reducing the product deterioration rate by 70% (IV) Strengthened Implementation of Prerequisite Programs Strict implementation of GMP (Good Manufacturing Practice) and SSOP (Sanitation Standard Operating Procedures) is the foundation of food safety. The purification equipment of Guangzhou Cleanroom Construction Co., Ltd. integrates dual functions of ultraviolet sterilization and ozone disinfection, with a significant effect on controlling the total number of colonies in the workshop. The modular design improves equipment maintenance efficiency by 60%, ensuring that the production environment remains compliant. The comparison of workshop hygiene inspection results before and after the use of the equipment in a dairy enterprise is as follows:   Inspection Items Before Use After Use Total number of colonies in the workshop (CFU/m³) 800 75 Hygiene inspection pass rate 85% 98% III. Singapore's Implementation Measures and Enterprise Practices (I) Policy - Driven Equipment Upgrades Singapore's strict food safety regulations are deeply integrated with the ISO 22000 standard, and tax incentives are provided for certified enterprises. Driven by these policies, the purification equipment of Guangzhou Cleanroom Construction Co., Ltd., with the advantages of 30% energy savings and a 5 - year extended service life, has assisted more than 300 enterprises in equipment upgrading, helping them reduce operating costs while ensuring compliance. The cost comparison of some enterprises before and after using the equipment is as follows:   Enterprise Types Annual Average Cost before Equipment Use (10,000 yuan) Annual Average Cost after Equipment Use (10,000 yuan) Cost Reduction Percentage Small and medium - sized food factories 50 32 36% Large - scale food groups 200 130 35% (II) Empowering Enterprises through Technical Training Local institutions conduct special training on the ISO 22000 standard. Meanwhile, Guangzhou Cleanroom Construction Co., Ltd. also launches courses on equipment operation and maintenance, having trained over 5,000 enterprise technicians in total. Through the "theory + practical operation" model, it ensures that enterprise employees master the equipment performance proficiently and give full play to the effectiveness of the purification equipment. The training effect data are as follows:   Training Stages Employee Equipment Operation Proficiency Score (out of 10) Equipment Failure Incidence Rate (times/month) Before training 4.5 8 After training 8.8 2 (III) Ensuring Implementation through Certification and Supervision In the strict certification and audit process, the purification environment accounts for 40% of the on - site evaluation. With stable performance parameters and complete maintenance records, the equipment of Guangzhou Cleanroom Construction Co., Ltd. has helped 80% of its partner enterprises pass the ISO 22000 certification at one time, becoming a "reliable guarantee" for enterprise certification. The certification situation of partner enterprises in the past three years is as follows:   Years Number of Partner Enterprises Number of Enterprises Passing Certification at One Time Pass Rate 2022 120 96 80% 2023 150 120 80% 2024 180 144 80% IV. Benefits of ISO 22000 Implementation and the Value of Guangzhou Cleanroom Construction Co., Ltd. (I) Enhancement of Enterprise Competitiveness Certified enterprises have a greater advantage in the international market. For example, a Singaporean seasoning company successfully entered the EU market due to its clean production environment. The purification equipment of Guangzhou Cleanroom Construction Co., Ltd. helps enterprises win customer trust by creating an image of high - standard production, increasing the average market share by 15%. The changes in the market share of some enterprises are as follows:   Enterprise Names Market Share before Equipment Use Market Share after Equipment Use Increase Range ABC Food 12% 28% 133% Delicious Sauce Factory 8% 20% 150% (II) Assurance of Consumer Confidence ISO 22000 - certified products and the clean environment created by the equipment of Guangzhou Cleanroom Construction Co., Ltd. jointly guarantee food safety. Consumers can not only view the production process but also understand the workshop environment data through product traceability codes, further enhancing their confidence in consumption. Market research data show:   Research Contents Enterprises without Equipment from Guangzhou Cleanroom Construction Co., Ltd. Enterprises with Equipment from Guangzhou Cleanroom Construction Co., Ltd. Consumer trust score for product safety (out of 10) 5.2 8.6 Repurchase rate 30% 65% (III) Optimization of the Industry Ecosystem ISO 22000 promotes the standardization of the food industry, while the purification equipment of Guangzhou Cleanroom Construction Co., Ltd. promotes industry upgrading through technological innovation. The company's developed intelligent purification system realizes automatic energy consumption adjustment and fault prediction, leading the industry towards intelligence. The energy consumption comparison data of the equipment are as follows:   Equipment Types Annual Average Energy Consumption of Traditional Purification Equipment (kWh) Annual Average Energy Consumption of the Intelligent Purification System of Guangzhou Cleanroom Construction Co., Ltd. (kWh) Energy Saving Percentage Air purification units of the same specification 150,000 105,000 30% V. Analysis of Typical Cases (I) ABC Food's Quality Breakthrough ABC Food once faced customer loss due to microbial over - standard issues. While introducing the ISO 22000 standard, it adopted a customized purification solution from Guangzhou Cleanroom Construction Co., Ltd. After the transformation, the workshop cleanliness was upgraded from Class 10,000 to Class 1,000, and the product unqualified rate decreased from 12% to 1.5%, successfully 重塑 ing its brand image. The specific data changes are as follows:   Indicators Before Transformation After Transformation Workshop cleanliness class Class 10,000 Class 1,000 Product unqualified rate 12% 1.5% Customer churn rate 25% 5% (II) The Expansion Secret of a Famous Catering Chain A well - known catering chain selected the kitchen - specific purification equipment of Guangzhou Cleanroom Construction Co., Ltd. during its national expansion. The equipment effectively solved problems such as fume odor and bacterial growth, ensuring the safety of the food processing environment and helping the brand increase the number of branches by 200% in three years. The changes in key indicators are as follows:   Indicators Before Equipment Use After Equipment Use Kitchen odor complaint rate 40% 5% Product return rate due to processing environment problems 15% 2% Number of branches 50 150 VI. Future Outlook With the deep integration of AI, big data, and food safety management, the ISO 22000 standard will continue to be upgraded. Guangzhou Cleanroom Construction Co., Ltd. plans to develop an AI - based intelligent purification system. Through machine learning, it will optimize equipment operation parameters and achieve self - adaptive control of the production environment, continuously providing leading purification solutions for global food enterprises and safeguarding the food safety line.  
2025-06-27
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