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Latest company case about Quality Management of Biopharmaceutical Workshop Projects: A Solid Defense for Drug Safety

Quality Management of Biopharmaceutical Workshop Projects: A Solid Defense for Drug Safety

In the field of biopharmaceuticals, the quality of workshop projects is directly related to drug safety and efficacy. Guangzhou Cleanroom Construction Co., Ltd. has been deeply engaged in the industry, using professional capabilities to build a solid foundation for quality management of biopharmaceutical workshop projects and providing escort for pharmaceutical production. I. Overall Layout of Quality Management Process (I) Control Preparation: Plan Before Acting Data collection is the foundation. Comprehensively sort out the regulatory standards, design drawings, equipment parameters, etc. involved in the biopharmaceutical workshop project to ensure that quality control is based on regulations. Develop exclusive control plans, and clarify quality objectives and control points in combination with the special requirements of biopharmaceuticals for cleanliness, sterile environment, etc. Establish a quality management system, from personnel responsibilities to operation specifications, to build a strict quality assurance network. Carry out control disclosures to make every person involved in the project clear about the quality standards and their own responsibilities, and gather quality consensus. (II) Before Construction: Multi - Dimensional Pre - control Pre - control of personnel, materials, and equipment comes first. Screen personnel with experience in biopharmaceutical workshop construction, conduct professional training to improve quality awareness and practical operation skills; strictly check materials and equipment, from basic materials such as air ducts to purification equipment, to ensure that they meet the quality requirements of cleanliness and sterility in biopharmaceuticals. Technical pre - control focuses on key points. For complex technical links such as the purification technology and pipeline layout of the biopharmaceutical workshop, organize expert demonstrations to optimize the construction technology plan. Plan pre - control refines the process, and detailedly plans the construction process and quality inspection nodes to build a solid framework for construction. Environmental pre - control cannot be ignored. Plan measures for cleaning, dust prevention, etc. of the construction environment in advance to avoid construction pollution affecting the subsequent cleanliness of the workshop. (III) During Construction: Dynamic Quality Protection Quality inspection runs through the whole process. Adopt the combination of patrol inspection and special inspection, and strictly inspect key processes such as air duct processing, installation, and purification equipment commissioning. Once deviations are found, rectify them immediately. Regularly hold quality meetings, bring together construction parties, supervision parties, and our technical personnel, report quality conditions, discuss and solve construction problems, and gather the joint force of quality control. Establish a defect management mechanism, timely record and track quality hazards and construction loopholes until closed - loop solutions are achieved. Simultaneously do a good job in data management, accurately record construction quality data and rectification situations, and provide strong support for quality traceability and subsequent acceptance. (IV) Completion Stage: Build the Last Line of Defense Self - acceptance is strict and meticulous. According to the quality standards of the biopharmaceutical workshop, verify key indicators such as air duct air leakage volume test and cleanliness detection one by one to ensure that the project quality meets the standards. Actively cooperate with external acceptance, such as acceptance by the drug supervision department and the customer. Sort out data in advance and rectify problems to ensure the smooth progress of acceptance. Completion delivery pays attention to details, do a good job in project data handover, operation training, etc., so that biopharmaceutical enterprises can receive and put into production smoothly with peace of mind. At the same time, continuously improve data collection to retain complete data for subsequent project review and quality improvement. II. Strong Execution in Quality Control Process - Taking Air Duct Project as an Example In the biopharmaceutical workshop, the air duct system is crucial for creating a clean environment. The company has built a strict quality control chain around the air duct project: Air Duct Processing Inspection: Strictly control the blanking accuracy and notch quality to ensure that the air duct is formed regularly and lay a foundation for subsequent quality. Air Duct Cleaning Inspection: Follow the cleanliness requirements of biopharmaceuticals, adopt professional cleaning processes to remove oil stains and impurities, and check the cleanliness of the inner wall of the air duct after cleaning to avoid polluting the air flow. Air Duct Gluing Inspection: Pay attention to the uniformity and tightness of the sealant to prevent air leakage from affecting the cleanliness of the workshop. Inspect the gluing quality section by section to build a solid sealing line of defense. Finished Air Duct Acceptance on Delivery: Check and verify the specifications, quantity, and re - measure the dimensional deviation. Combined with light leakage detection, check the air duct for damage and leakage points to prevent unqualified air ducts from entering the construction link. Air Duct Air Leakage Volume Test: As a key acceptance item, simulate the operating conditions of the biopharmaceutical workshop, accurately detect the air leakage of the air duct, and ensure the stable delivery of clean air flow.   Taking a glimpse of the air duct project, Guangzhou Cleanroom Construction Co., Ltd. has created a reliable quality foundation for biopharmaceutical workshop projects with full - process and strong - execution quality management. In the future, the company will continue to deeply engage in the industry, keep up with the development of the biopharmaceutical industry, iterate the quality management model, contribute more to safeguarding drug quality safety and promoting the high - quality development of the pharmaceutical industry, and make every biopharmaceutical workshop a solid fortress for drug safety.  
2025-06-11
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Latest company case about Ventilation and Exhaust Systems in Biopharmaceutical Cleanroom Engineering

Ventilation and Exhaust Systems in Biopharmaceutical Cleanroom Engineering

Design and Standards for Laboratory Ventilation and Exhaust Systems I. Definition of Laboratory Ventilation and Exhaust Systems The ventilation and exhaust system in biopharmaceutical cleanroom engineering refers to a scientifically designed airflow organization and pressure control system that ensures indoor air quality meets cleanliness requirements. Its core functions include: controlling pollutant diffusion, maintaining pressure differential gradients, ensuring personnel safety, and stabilizing the experimental environment. According to international standards ISO 14644-1 and WHO GMP requirements, the system must achieve precise control of directional airflow (from clean areas to contaminated areas) and air changes per hour (ACH). II. System Components and Key Technologies 1. Air supply system: Uses HEPA (High-Efficiency Particulate Air filters, compliant with EN 1822 standards) or ULPA filters, with filtration efficiency required to exceed 99.99% (for 0.3μm particles).2. Exhaust system: For biosafety laboratories (BSL-2/3 levels), BIBO (Bag-In/Bag-Out) filters and chemical disinfection devices must be installed, complying with NSF/ANSI 49 standards.3. Airflow organization: Employs unidirectional (laminar) or non-unidirectional (turbulent) airflow designs, with clean area air velocity typically at 0.45±0.1 m/s (ISO 14644-3).4. Pressure control: Uses VAV (Variable Air Volume) valves for dynamic pressure differential adjustments, with adjacent zone pressure differentials ≥5 Pa (EU GMP Annex 1). III. International Standards and Design Guidelines • ASHRAE 110-2016 (USA): Specifies performance testing methods for ventilation systems.• EU GMP Annex 1: Defines pressure differential and air change requirements for sterile drug manufacturing environments.• China GB 50457-2019: Design standards for cleanrooms in pharmaceutical industries.• Key parameters: Biosafety cabinet exhaust must be independently configured, with exhaust duct negative pressure ≥-250 Pa (CDC/NIH Biosafety in Microbiological Laboratories). IV. Requirements for Special Applications 1. High-potency drug production areas: Exhaust air must undergo two-stage HEPA filtration (EU GMP Appendix 3).2. Virus-handling laboratories: Exhaust systems must feature in-situ leak detection (ISO 14644-3 Appendix B).3. Energy-efficient design: When heat recovery devices are used, cross-contamination risks must be eliminated (ASHRAE 170-2017).
2025-06-11
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Latest company case about Laboratory Furniture for Biopharmaceutical Cleanroom Engineering

Laboratory Furniture for Biopharmaceutical Cleanroom Engineering

1. Definition of Laboratory Furniture for Biopharmaceutical Cleanroom Engineering Laboratory furniture for biopharmaceutical cleanroom engineering refers to specialized furniture designed for clean environments, meeting stringent requirements for cleanliness, corrosion resistance, and sterility in biopharmaceutical production, research, and quality control. Such furniture is typically made of materials like stainless steel or epoxy resin, featuring easy cleaning, dustproof, and antibacterial properties. 2. Main Types and Features 1. Cleanroom Laboratory Benches: Provide a localized clean environment for aseptic operations; 2. Biological Safety Cabinets: Protect operators and the environment from biohazards; 3. Cleanroom Storage Cabinets: Safely store materials and reagents in clean environments; 4. Cleanroom Laboratory Workbenches: Corrosion-resistant and easy-to-clean work surfaces; 5. Cleanroom Pass Box: Enable safe transfer of materials between different cleanliness zones. 3. Design Standards and Requirements Laboratory furniture for biopharmaceutical cleanroom engineering must comply with the following international standards: · ISO 14644-1 Cleanrooms and Associated Controlled Environments · GMP (Good Manufacturing Practice) · USP Standards for Handling Hazardous Drugs · EN 12469 Performance Standards for Biological Safety Cabinets · FDA 21 CFR Part 11 Electronic Records and Electronic Signatures. 4. Material Selection 1. Stainless Steel: 304 or 316L stainless steel, corrosion-resistant and easy to clean; 2. Epoxy Resin: Seamless and chemically resistant; 3. Tempered Glass: Used for observation windows and barriers; 4. Special Coatings: Antibacterial and antistatic coatings. 5. Installation and Maintenance 1. Installation must be performed under cleanroom conditions; 2. Regular cleaning and disinfection; 3. Periodic checks for sealing integrity and airflow patterns; 4. Filter replacement based on usage frequency. Guangzhou Cleanroom Construction Co., Ltd.
2025-06-11
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Latest company case about What is an enclosed structure?

What is an enclosed structure?

Guangzhou Cleanroom Construction Co., Ltd. 1、Definition of Enclosed Structure An enclosed structure refers to the physical barriers that separate the controlled environment from the external surroundings in cleanroom and purification engineering applications. These structures are designed to maintain specific environmental conditions including temperature, humidity, air pressure, and particulate levels. 2、Key Components The main components of an enclosed structure in purification engineering include: Component Function Material Walls Primary separation barrier Sandwich panels, steel, glass Ceiling Air distribution and lighting support Perforated panels, HEPA filters Floor Load bearing and cleanability Epoxy, PVC, raised flooring Doors & Windows Access while maintaining separation Air-tight designs with seals 3、International Standards Enclosed structures in cleanroom applications must comply with various international standards including: ISO 14644-1: Classification of Air Cleanliness ISO 14644-4: Design, Construction and Start-up EU GMP Annex 1: Manufacture of Sterile Medicinal Products FDA Guidance for Industry: Sterile Drug Products 4、Design Considerations Key design factors for effective enclosed structures include: Air tightness to prevent contamination Material compatibility with cleaning agents Structural integrity under pressure differentials Modularity for future expansion Integration with HVAC systems 5、Importance in Purification Engineering As a purification engineering company owner, I emphasize that the enclosed structure is the foundation of any controlled environment system. It directly impacts: Energy efficiency of the cleanroom Long-term maintenance costs Consistency of environmental parameters Compliance with regulatory requirements Product quality and process reliability  
2025-06-09
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Latest company case about Introduction to Flooring Engineering

Introduction to Flooring Engineering

— A Key Component in Cleanroom Engineering Definition of Flooring Engineering Flooring engineering refers to the systematic process of designing, constructing, and maintaining building floors, involving techniques such as concrete base treatment, wear-resistant layer installation, and anti-static coatings. According to the ISO 9001:2015 Quality Management System standards, flooring engineering must meet three core criteria: functionality, durability, and safety. Special Requirements in Cleanroom Engineering In cleanroom engineering (referencing ISO 14644-1 standards), flooring must possess: • Dust-free and non-shedding properties (compliant with FS209E standards) • Chemical corrosion resistance (tested per ASTM D1308) • Conductive/anti-static functionality (per IEC 61340-5-1 standards) Application Characteristics in the Myanmar Market To accommodate Myanmar's hot and humid climate (average humidity >80%), we employ flooring construction techniques based on the German DIN 18560 standard, with emphasis on: (1) Moisture barrier treatment (thickness ≥0.2mm) (2) High-temperature-resistant epoxy coatings (withstands up to 50°C) (3) Anti-mold and antibacterial additives (compliant with ISO 22196 standards) Project Acceptance Standards Strict adherence to international triple acceptance standards: • Flatness (≤2mm gap under a 3m straightedge) • Compressive strength (≥25MPa, per EN 13892 standards) • Cleanliness (particle counting method, ISO 14644-3)  
2025-06-09
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Latest company case about Electrical System of Biopharmaceutical Workshop Engineering - Strong Current Power Distribution Equipment

Electrical System of Biopharmaceutical Workshop Engineering - Strong Current Power Distribution Equipment

In the biopharmaceutical industry, strong current power distribution equipment serves as a critical backbone for ensuring stable production operations. Its performance and reliability directly impact the quality and efficiency of drug manufacturing. Compared to other industrial scenarios, biopharmaceutical workshops impose more stringent requirements on power distribution equipment, demanding both high-load, long-term operation and stable, safe power supply. Below, we delve into the innovations and developments of strong current power distribution equipment in biopharmaceutical workshops. I. Intelligent Monitoring: The 'Vision and Hearing' of Power Distribution Equipment The intelligent monitoring system of power distribution equipment establishes a precise power sensing network through IoT and edge computing technologies. Built-in MEMS sensor arrays not only collect basic power parameters (voltage, current, etc.) at a frequency of 100 times per second but also detect early fault signals (e.g., insulation aging, poor contact) via partial discharge detection. After preliminary analysis by edge computing units, abnormal data is transmitted to the central control system in milliseconds via 5G networks.   1. Technology Core: Digital twin technology is used in the visualization monitoring platform to simulate real-time equipment operation. 2. Application Case: A biopharmaceutical enterprise detected a 0.5°C abnormal temperature rise in a transformer through this system, triggering an early warning 72 hours in advance and locating a cooling fan failure, thereby avoiding equipment damage and production downtime, with direct economic loss reduction exceeding ¥2 million. 3. Data Accuracy: The system achieves millisecond-level data transmission and sub-1% parameter monitoring accuracy. II. Dynamic Regulation: The 'Adaptive Engine' of Power Supply The dynamic regulation system integrates AI prediction algorithms and power electronics technology to achieve millisecond-level response. By analyzing three years of production data, the system accurately predicts power demand curves for different processes.   1. Hierarchical Power Supply: During the vaccine fermentation stage, the system prioritizes 100% power supply to core equipment (stirring motors, temperature control systems) while dynamically adjusting non-critical equipment (e.g., lighting) to 70% power. 2. Energy Efficiency Data: After deploying this system in an insulin production workshop, peak power utilization increased by 40%, and overall energy consumption decreased by 32%. 3. Communication Technology: Power line carrier communication ensures inter-device command transmission delays of
2025-06-09
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Latest company case about Electrical System of Biopharmaceutical Workshop Engineering - Refrigeration Station Group System

Electrical System of Biopharmaceutical Workshop Engineering - Refrigeration Station Group System

In biopharmaceutical workshops, the refrigeration station group system is as crucial as the human body's thermoregulatory system is to maintaining life. The production process of biopharmaceuticals has extremely stringent requirements for environmental conditions such as temperature and humidity. The refrigeration station group system shoulders the important task of ensuring a stable production environment and guaranteeing the quality and safety of drugs. If the temperature control is improper, the active ingredients of drugs may become inactive, and the cultivation environment for microorganisms may be damaged, thereby affecting the efficacy of drugs. In severe cases, it may even lead to the scrapping of an entire batch of drugs, causing huge losses. I. Composition of the Refrigeration Station Group System (I) Chiller Units: The Core of Refrigeration Chiller units can be regarded as the "heart" of the refrigeration station group system. Through a series of refrigeration cycles including compression, condensation, throttling, and evaporation, they compress low-temperature and low-pressure refrigerant gas into high-temperature and high-pressure gas. After heat dissipation in the condenser, it becomes high-pressure liquid, and then the pressure is reduced through the throttling device. In the evaporator, it absorbs the heat of the chilled water, reducing the temperature of the chilled water and bringing "coolness" to the workshop. In biopharmaceutical workshops, centrifugal chiller units are commonly used because of their large cooling capacity and high efficiency, which meet the high demand for cooling capacity in large-scale production. (II) Pumps: The Drivers of Circulation Pumps are like the "blood vessels" of the refrigeration station group system, responsible for pushing the chilled water and cooling water to circulate within the system. The chilled water pumps transport the low-temperature chilled water to various areas in the workshop that require refrigeration. After absorbing heat and increasing in temperature, it is sent back to the evaporator of the chiller unit for recooling. The cooling water pumps transport the cooling water that has absorbed heat from the condenser to the cooling tower for heat dissipation and temperature reduction, and then it returns to the condenser for recycling. Nowadays, variable-frequency pumps are widely used in biopharmaceutical workshops. They can automatically adjust the rotation speed according to the system load, achieving significant energy-saving effects. They can also precisely control the water flow, ensuring the stable operation of the system. (III) Cooling Towers: Key Heat Dissipation Equipment Cooling towers can be called the "heat dissipation masters" of the refrigeration station group system. Their main function is to dissipate the heat carried by the cooling water into the atmosphere, reducing the temperature of the cooling water. In biopharmaceutical workshops, counterflow cooling towers are often used. They utilize the counterflow of air and water to increase the contact area and time, achieving efficient heat dissipation. At the same time, the cooling towers are equipped with intelligent control systems, which can automatically adjust the rotation speed of the fans according to the ambient temperature and the temperature of the cooling water, ensuring the heat dissipation effect while saving electricity. II. Operation Mechanism of the Refrigeration Station Group System (I) Intelligent Group Control Technology: The "Smart Brain" of the System Intelligent group control technology endows the refrigeration station group system with "intelligence" and serves as the "brain" of the entire system. It collects data such as the temperature, humidity, and cooling load of the workshop in real-time through sensors, as well as the operation parameters of equipment such as chiller units, pumps, and cooling towers. Using advanced algorithms for analysis and processing, it precisely controls the operation status of each device. For example, when the cooling load of the workshop decreases, the intelligent group control system will automatically reduce the number of operating chiller units and lower the rotation speeds of the pumps and cooling tower fans, minimizing energy consumption while meeting the refrigeration demand. (II) Load Regulation Strategy: Precise Adaptation to Requirements In biopharmaceutical workshops, the cooling load requirements of different production processes fluctuate greatly. The refrigeration station group system adopts flexible load regulation strategies to precisely adapt to these changes. Chiller units have multi-stage energy regulation functions and can automatically adjust the cooling capacity output according to the size of the cooling load. Pumps and cooling tower fans can also change the flow rate and air volume through variable-frequency speed regulation to achieve dynamic matching with the cooling load. For instance, during the drug fermentation stage, which has high requirements for temperature control and a large cooling load demand, the system will operate at full capacity. In the drug packaging stage, when the cooling load demand is small, the system will automatically operate with reduced energy consumption. III. Innovative Technological Applications of the Refrigeration Station Group System (I) Internet of Things (IoT) Technology: Achieving Remote Monitoring and Management IoT technology has brought the refrigeration station group system into a new era of remote monitoring and management. By installing intelligent sensors and communication modules on the equipment, the operation data of the equipment is uploaded to the cloud platform in real-time. Managers can view the operation status of the system anytime and anywhere through terminals such as mobile phones and computers, operate the equipment remotely, and handle fault alarms in a timely manner. This not only improves management efficiency but also enables the prediction of potential equipment failures in advance, facilitating preventive maintenance and reducing downtime. (II) Big Data Analysis and Predictive Maintenance: Ensuring Stable Equipment Operation The application of big data analysis technology in the refrigeration station group system provides a safeguard for the stable operation of the equipment. The system collects a large amount of historical operation data of the equipment and uses big data analysis algorithms to uncover the patterns behind the data and establish equipment performance models. By comparing the real-time data with the predicted values of the models, potential fault hazards of the equipment can be detected in advance, and preventive maintenance can be arranged. For example, if it is predicted that the bearing of a certain pump may fail in a week, maintenance and replacement can be arranged in advance to avoid production interruptions caused by sudden failures. IV. Advantages of the Refrigeration Station Group System (I) High Efficiency and Energy Saving: Reducing Operating Costs The refrigeration station group system achieves high efficiency and energy saving through the application of intelligent group control technology, load regulation strategies, and energy-saving equipment, significantly reducing the operating costs of biopharmaceutical workshops. Compared with traditional refrigeration systems, it can save 30% - 50% of energy consumption. Taking a large biopharmaceutical workshop as an example, it can save several million yuan in electricity bills every year. In the long run, the economic benefits are remarkable. (II) Precise Temperature Control: Guaranteeing Drug Quality Precise temperature control is the lifeline of biopharmaceutical workshops, and the refrigeration station group system performs excellently in this regard. It can control the temperature of the workshop within ±0.5°C and the humidity within ±5%, providing a stable environment for drug production. During the vaccine production process, precise control of temperature and humidity can ensure the activity and stability of the vaccine, improving the quality and safety of drugs. V. Key Points of Maintenance and Management of the Refrigeration Station Group System (I) Regular Inspections and Maintenance: Extending Equipment Lifespan Regular inspections and maintenance are the keys to ensuring the long-term stable operation of the refrigeration station group system and extending the lifespan of the equipment. Maintenance personnel need to conduct comprehensive inspections of equipment such as chiller units, pumps, and cooling towers according to the specified inspection cycles, including equipment appearance, operation parameters, and connecting components. Regularly add lubricating oil to the equipment, replace vulnerable parts, and clean the condensers and evaporators. Generally, chiller units are comprehensively maintained once a quarter, and pumps and cooling towers are inspected and maintained once a month. (II) Fault Diagnosis and Troubleshooting: Quickly Restoring Production When a fault occurs in the refrigeration station group system, quick and accurate fault diagnosis and troubleshooting are of great importance. Maintenance personnel should rely on the built-in fault diagnosis system of the equipment, data from intelligent sensors, and their own experience to quickly determine the cause and location of the fault. For common faults such as pump motor overload and cooling tower fan failure, spare parts should be prepared for timely replacement and repair. For complex faults, technical support from the manufacturer should be contacted in a timely manner to restore the normal operation of the system as soon as possible and minimize the impact on production.  
2025-06-09
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Latest company case about Intelligent Energy Monitoring System for Biopharmaceutical Workshops: Reconstructing the Smart DNA of Electrical Control

Intelligent Energy Monitoring System for Biopharmaceutical Workshops: Reconstructing the Smart DNA of Electrical Control

In the precision operation of biopharmaceutical workshops, the electrical system is not only the power source but also the "nerve center" of aseptic production. From kilowatt-level energy regulation of freeze-dryers to microamp-level leakage monitoring in clean zones, energy efficiency and intelligent control precision directly determine GMP compliance and production costs. With deep expertise in overseas pharmaceutical engineering, Guangzhou Cleanroom Construction Co., Ltd. introduces the Intelligent Energy Monitoring System, featuring a three-in-one architecture of "real-time digital twin + adaptive control + remote operation," to create an energy-efficient, safe, and compliant electrical ecosystem for biopharmaceutical workshops. I. Reconstructing Three Core Pain Points of Biopharmaceutical Electrical Systems 1. Conflict Between Energy Black Holes and Compliance Red Lines Freeze-drying and sterilization equipment account for 65% of workshop energy consumption. Traditional power distribution systems fail to dynamically match process loads, leading to 15%-20% energy waste. FDA 21 CFR Part 11 requires traceability of critical energy data, but manual meter reading has an error rate of up to 8%, failing to meet real-time audit requirements. 2. Isolated Equipment and Lagging Fault Response Electrical devices such as transformers, UPS, and air conditioning units operate independently, with an average delay of 2 hours in detecting anomalies. Hidden faults in explosion-proof electrical systems in clean zones (e.g., insulation aging, harmonic pollution) may trigger cascading safety risks. 3. Challenges of Transnational Operation and Local Regulation Overseas projects must adapt to different voltage standards (e.g., EU 230V/50Hz, North America 480V/60Hz), but traditional control systems have poor compatibility. Regulations such as GMP and OSHA impose strict requirements on real-time monitoring of electrical safety parameters (e.g., grounding resistance ≤1Ω, leakage action time ≤0.1s). II. Three Core Technical Breakthroughs of the Intelligent System ▍ 1. Full-Time Domain Digital Twin: From "Experience Control" to "Digital Prediction" ▶ Millisecond-Level Data Acquisition Network Deploy LoRaWAN wireless sensors (accuracy: voltage ±0.5%, current ±0.2%) covering three levels of nodes: power distribution rooms, clean zones, and process equipment. Edge computing gateways developed in-house parse data in real time and upload it to a cloud-based digital twin platform, constructing a 3D dynamic model of the workshop's electrical system. ▶ AI Energy Efficiency Optimization Engine Dynamic load balancing: Predicts equipment energy peaks based on process work orders and automatically adjusts transformer tap changers and UPS output. For example, reactive power loss during the heating phase of freeze-dryers can be reduced by 12%. Harmonic governance closed loop: Automatically compensates for filters by capturing real-time signals of THD (total harmonic distortion) ≥5%, extending the lifespan of precision instruments by over 20%. ▶ Automatic Compliance Audit The system presets regulatory parameter thresholds (e.g., FDA, EU GMP). When clean zone illuminance is below 300lux or grounding resistance >1Ω, it automatically generates audit reports and triggers rectification processes. ▍ 2. Adaptive Control Network: Empowering Equipment with "Autonomous Thinking" ▶ Three-Level Control Architecture Design Control Level Core Function Technical Configuration Field Level Local equipment protection (overvoltage/undervoltage/leakage), response time 10Pa, the air supply motor frequency is adjusted to reduce fan energy consumption by 15%. ▍ 3. Global Remote Operation and Maintenance: Building a "Zero-Time-Difference" Control System ▶ Multi-Terminal Interaction Platform PC 端 (PC Terminal): 3D visualization interface for real-time monitoring of 100+ electrical parameters, supporting historical data retrieval (accuracy to 1 minute). 移动端 (Mobile Terminal): WeChat/APP pushes critical alarms (e.g., cable temperature >60°C, circuit breaker switching anomalies) with a response time
2025-06-06
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Latest company case about Automatic Control of Electrical Systems in Biopharmaceutical Workshop Engineering: Innovation Driving Production Transformation

Automatic Control of Electrical Systems in Biopharmaceutical Workshop Engineering: Innovation Driving Production Transformation

I. Key Technologies of Automatic Control of Electrical Systems in Biopharmaceutical Workshops​ Programmable Logic Controllers (PLCs) play the role of the central nervous system in biopharmaceutical workshops. They can precisely control various types of equipment in the workshop, such as fermenters, filling machines, and sterilization equipment. Through pre-set program logic, PLCs can automatically adjust the operating parameters of equipment according to the real-time requirements of the production process, ensuring the stability and consistency of the production process. For example, in the fermentation process, PLCs can monitor key parameters such as temperature, pH value, and dissolved oxygen content in the fermenter in real time, and automatically control the operation of heating, stirring, aeration, and other equipment according to pre-set thresholds, maintaining the optimal fermentation environment and ensuring the stability of drug quality. ​ Sensors are like the "senses" of biopharmaceutical workshops, providing key data support for the automatic control system. Various types of sensors, including temperature and humidity sensors, pressure sensors, flow sensors, and biomass sensors, are widely distributed throughout the workshop to comprehensively monitor the production environment and process. In the environmental control of cleanrooms, temperature and humidity sensors provide real-time feedback on indoor temperature and humidity data. The automatic control system adjusts the operation of the air conditioning system based on this data to ensure that the cleanroom always meets the environmental requirements for drug production. The high precision and reliability of sensors are the basis for achieving the accuracy of automatic control of electrical systems.​ Industrial Ethernet serves as the highway for data transmission between equipment in biopharmaceutical workshops, as well as between the control system and the management layer, ensuring the rapid and accurate transfer of information. It connects equipment such as PLCs, sensors, and host computers into an organic whole, enabling real-time data sharing and interaction. During the production process, equipment operation data can be quickly uploaded to the monitoring center through industrial Ethernet. Managers can grasp the production status in real time and issue control commands via the network, realizing remote monitoring and management. This efficient communication network significantly improves production coordination efficiency and provides strong support for the intelligent operation of the workshop.​ (I) Improving Production Quality and Consistency​ (II) Enhancing Production Efficiency and Capacity​ (III) Reducing Energy Consumption and Operating Costs​ III. Challenges and Countermeasures​ Biopharmaceutical workshops involve various types of equipment and control systems, and achieving seamless integration between systems faces many challenges. The communication protocols and interface standards of different equipment suppliers may vary, increasing the difficulty of system integration. To address this challenge, at the project planning stage, unified technical standards and interface specifications need to be formulated, requiring equipment suppliers to design and manufacture equipment in accordance with the standards. At the same time, advanced system integration technologies and tools, such as middleware technology, are adopted to achieve data conversion and communication coordination between different systems, ensuring the compatibility and stability of the entire automatic control of electrical systems.​ With the digital transformation of biopharmaceutical workshops, the generation and transmission of a large amount of production data pose risks to data security and privacy protection. Production data contains the core technology and trade secrets of enterprises. Once leaked, it will cause huge losses to enterprises. Therefore, a complete data security protection system needs to be established. Encryption technology is used to ensure the security of data during transmission and storage. Strict user permission management is set up to limit the access levels of different personnel to data. Network security devices such as firewalls and intrusion detection systems are deployed to prevent external illegal attacks and ensure the security and integrity of production data.​ The automatic control of electrical systems in biopharmaceutical workshop engineering involves knowledge from multiple fields, such as automation, information technology, and biopharmaceutical processes, and requires a high comprehensive quality of professional talents. Currently, the shortage of such interdisciplinary professional talents in the industry restricts the promotion and application of automatic control technologies. Enterprises should strengthen cooperation with universities and scientific research institutions, carry out customized talent training programs, and provide students with practical opportunities so that they can master interdisciplinary knowledge and skills. At the same time, enterprises should strengthen employee training internally, regularly organize technical exchanges and training courses, improve the professional level of existing employees, and build a high-quality team of professional talents to provide talent support for the stable operation of automatic control of electrical systems.​ Take a large biopharmaceutical enterprise as an example. Its newly built biopharmaceutical workshop introduced an advanced automatic control solution for electrical systems. By constructing a control system with PLC as the core, combined with high-precision sensors and an industrial Ethernet communication network, the full automation of the production process was achieved. In terms of production quality, the batch consistency of drugs was significantly improved, and the product qualification rate increased from the previous 90% to over 98%. Production efficiency was greatly improved, with a 50% increase in production capacity and a 30% reduction in energy consumption. When dealing with the challenges of system integration, the enterprise closely cooperated with equipment suppliers to unify technical standards and successfully achieved the integration of various systems. By establishing a complete data security protection system, the security of production data was effectively guaranteed. In addition, the enterprise actively cultivated professional talents, and the internal technical team was able to proficiently handle various problems in system operation, ensuring the efficient and stable operation of the workshop and bringing significant economic benefits and market competitiveness to the enterprise.​      
2025-06-06
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Latest company case about Hospital Central Supply Room Stainless Steel Platform Stand Design (1200×550×200mm)

Hospital Central Supply Room Stainless Steel Platform Stand Design (1200×550×200mm)

Application Background This stainless steel platform stand is designed for hospital central supply rooms, providing a sterile, durable, and easy-to-clean support solution for medical equipment, sterilization trays, and instrument storage. Its corrosion-resistant structure meets the strict hygiene requirements of medical environments. Design Specifications 1. Dimensions & Structure Overall size: 1200mm (L) × 550mm (W) × 200mm (H) Optimized for sterilization carts, instrument trays, and medical device placement Low-profile design (200mm height) ensures stability while allowing easy access Frame material: 38×38×1.0304 stainless steel square tube High strength & rigidity to support heavy medical equipment Smooth, non-porous surface prevents bacterial accumulation Resistant to chemicals, moisture, and high-temperature sterilization 2. Adjustable Feet (4 Units) Stainless steel or nylon adjustable feet for stability on uneven floors Anti-slip & vibration-damping to prevent equipment movement Easy height adjustment for leveling on hospital flooring Key Advantages for Medical Use ✔ Hygienic Design – Easy to disinfect with hospital-grade cleaners; no rust or corrosion✔ Heavy-Duty Load Capacity – Supports sterilization containers, surgical instrument trays, and medical devices✔ Smooth, Seamless Welding – No crevices for bacteria or contaminants to accumulate✔ Mobility-Friendly – Compatible with medical carts and trolleys when needed Customization Options Electropolished or antimicrobial-coated finishes Additional support bars for heavier loads Locking casters (optional) for mobile use This medical-grade stainless steel platform stand is an ideal solution for central sterile supply departments (CSSD), operating rooms, and laboratory settings. For specialized hospital requirements, contact us for tailored solutions. Contact us for quotes, technical drawings, and customization!    
2025-06-24
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Latest company case about Electric Lift Pass Box Design Solution: The Perfect Integration of Safety, Intelligence, and Efficiency

Electric Lift Pass Box Design Solution: The Perfect Integration of Safety, Intelligence, and Efficiency

In modern clean environments such as laboratories, hospitals, pharmaceutical factories, and food processing facilities, pass boxes are critical equipment for transferring items. Their performance directly impacts work efficiency and environmental cleanliness. Today, I will introduce an advanced electric lift pass box design that incorporates multiple user-friendly features and safety considerations. Core Materials and Structural Design The main frame of this pass box is constructed from high-quality SUS304 stainless steel, which offers excellent corrosion resistance and structural strength while meeting the high surface requirements of clean environments. The stainless steel surface undergoes special treatment for easy cleaning and disinfection, ensuring it remains rust-free and deformation-free even after long-term use. The glass door features an innovative design combining a stainless steel pipe frame with 5mm thick 3C tempered glass. This configuration ensures both visual transparency and structural stability. The 5mm tempered glass is not only highly durable but also breaks into small, harmless particles in the unlikely event of damage, significantly reducing safety risks. Intelligent Lift System This solution provides two lift control modes to suit different scenarios: l One-Touch Lift Mode: Simple and straightforward, ideal for routine item transfers. l Sensor-Activated Lift Mode: Smart and convenient, automatically opening when an operator approaches. A notable feature is the dual-side lift control design, where the master control side can remotely operate the lift function on the opposite side. This is particularly useful in environments requiring strict isolation, allowing operators to coordinate transfers without frequent movement. Safety Protection Features Safety is always our top priority. This pass box is equipped with an infrared anti-pinch sensor system, which immediately stops the lifting motion upon detecting an obstacle, effectively preventing hand injuries or damage to objects. This feature is especially beneficial in busy workplaces with frequent transfers. Applications and Advantages This electric lift pass box is ideal for the following environments: l Biosafety laboratories l Item transfers between hospital operating rooms and pharmacies l Clean zones in food and pharmaceutical production l Dust-free workshops for electronic components Compared to traditional pass boxes, this solution offers significant advantages: l More convenient operation with reduced human contact l Enhanced safety to prevent accidents l Better sealing to maintain cleanliness l High durability with long-term resistance to deformation Conclusion This electric lift pass box design combines premium materials, intelligent control, and multiple safety protections, representing the future of pass box technology. Whether evaluated for ease of use, safety performance, or long-term durability, it is a high-quality solution worth considering. For facilities requiring high-standard cleanliness and efficient workflows, this design ensures notable improvements in both productivity and safety.  
2025-06-24
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Latest company case about 2017 Design Standards for Food Factories: The Cornerstone of Food Safety Production

2017 Design Standards for Food Factories: The Cornerstone of Food Safety Production

In the food industry, the safety and standardization of the production environment are directly related to consumers' health. Singapore Standard SS 585:2017 Design Standards for Food Factories serves as a crucial guideline for the construction and renovation of food factories in Singapore, safeguarding food safety from multiple dimensions. Guangzhou Cleanroom Construction Co., Ltd. has conducted in-depth research on and actively implemented this standard, leveraging its professional capabilities to assist food enterprises in creating compliant and efficient production spaces.​ I. In-depth Interpretation of the Core Provisions of SS 585:2017​ The SS 585:2017 standard covers various aspects of food factories, including site selection, layout, facilities and equipment, and hygiene management. These provisions work in tandem to establish a rigorous defense line for food safety production.​ (I) Site Selection Requirements​ ​ Clause Classification​ Specific Requirements​ Key Data/Indicators​ Design Principles​ Site Selection Requirements​ Keep a distance from pollution sources such as waste disposal sites and chemical plants; the terrain should be higher than the surrounding areas to prevent waterlogging​ Distance from pollution sources should be ≥ 500 meters; terrain height difference is recommended to be ≥ 0.5 meters​ Prevent external pollutants from entering the factory through air, water, and other means, which may affect food raw materials and the production environment. A higher terrain is conducive to natural drainage, reducing the impact of floods on the factory​ ​ (II) Workshop Layout​ Regarding workshop layout, in addition to clearly separating production areas, storage areas, and office areas, and having independent pedestrian and logistics channels, the cleanliness levels of different functional areas also need to match production requirements. For example, the cleanliness level of food processing areas is usually higher than that of raw material storage areas. Meanwhile, the setup of buffer zones between areas is of great importance. Buffer zones should be equipped with handwashing and disinfection facilities, air showers, etc., effectively preventing pollutants carried by personnel and materials from entering high - cleanliness areas.​ ​ Clause Classification​ Specific Requirements​ Key Data/Indicators​ Design Principles​ Workshop Layout​ Clearly separate production areas, storage areas, and office areas; have independent pedestrian and logistics channels; set up buffer zones in different functional areas​ Physical partitions are required for separation of different functional areas; the width of the channels should be ≥ 1.5 meters; the area of the buffer zone should be ≥ 6 square meters​ Physical partitions and independent channels avoid cross - contamination of pedestrians and logistics; buffer zones can purify personnel and materials entering high - cleanliness areas​ ​ (III) Air Purification​ Air purification in clean workshops is the key to ensuring food safety. SS 585:2017 stipulates that the cleanliness of areas in direct contact with food is recommended to reach ISO Class 8. To achieve this goal, not only high - efficiency filters are required, but also a reasonable design of air flow organization. Turbulent flow cleanrooms usually adopt a top - supply and bottom - return air flow form, which can effectively dilute indoor pollutants; while unidirectional flow cleanrooms discharge pollutants quickly through the principle of piston flow.​ ​ Clause Classification​ Specific Requirements​ Key Data/Indicators​ Design Principles​ Air Purification​ Clean workshops need to reach the corresponding cleanliness level; regularly detect air cleanliness and microbial content​ The cleanliness of areas in direct contact with food is recommended to reach ISO Class 8; conduct a comprehensive inspection at least once a quarter​ High - efficiency filtration and scientific air flow organization ensure clean air, and regular inspections ensure that the purification effect remains up to standard​ ​ (IV) Temperature and Humidity Control​ Different types of food have varying requirements for temperature and humidity. Take the baking industry as an example. The raw material storage area needs to be kept dry, with a humidity control of 50% - 60% to prevent raw materials such as flour from getting damp and caking. In the cold storage area of meat processing, the temperature should be controlled at 0 - 4°C, and the humidity at 60% - 70%, which can not only inhibit the growth of microorganisms but also prevent meat from dehydration and deterioration.​ ​ Clause Classification​ Specific Requirements​ Key Data/Indicators​ Design Principles​ Temperature and Humidity Control​ Set appropriate temperature and humidity ranges according to the type of food; the fluctuation range of temperature and humidity needs to be within a controllable interval​ Temperature control in the cold storage area at 0 - 4°C, humidity at 60% - 70%; temperature fluctuation ± 1°C, humidity fluctuation ± 5%​ Precise temperature and humidity control creates a suitable environment for food storage and processing, reducing the risk of quality changes​ ​ (V) Drainage System​ The slope design of drainage pipes directly affects drainage efficiency. A slope of ≥ 2% for drainage pipes ensures the rapid discharge of sewage, preventing water accumulation and the breeding of bacteria. At the same time, filters and P - traps should be installed at drainage outlets. Filters can intercept solid waste to prevent pipe blockages, and P - traps can prevent the backflow of odors and harmful gases from the sewer into the workshop.​ ​ Clause Classification​ Specific Requirements​ Key Data/Indicators​ Design Principles​ Drainage System​ Drainage pipes need to have a slope to prevent water accumulation; install filters and P - traps at drainage outlets​ The slope of drainage pipes should be ≥ 2%; the pore size of the filter should be ≤ 5mm​ Reasonable slope and drainage outlet facilities ensure smooth drainage and prevent workshop environmental pollution​ ​ II. Rich Application Examples and Remarkable Effects of the Standard​ (I) Renovation Project of a Baking Food Factory in Singapore​ Before the introduction of the SS 585:2017 standard, the factory had several problems. The raw material storage area was too close to the processing area, and there was no effective partition, so raw materials like flour were prone to absorbing odors generated in the processing area. The workshop ventilation system was imperfect, resulting in high air humidity, and some baked products became damp.​ After re - planning according to the standard, the raw material storage area was moved to an independent area, and moisture - proof and odor - proof partition doors were installed. A fresh air system combined with high - efficiency filters was adopted to improve the air quality in the workshop and strictly control the humidity. Meanwhile, the production process was optimized to enable a one - way flow of raw materials from the storage area to the processing area and then to the finished product area. After the renovation, the damp rate of products decreased from 12% to 3%, and the odor complaint rate decreased by 85%. The production environment was greatly improved, and product quality was significantly enhanced. ​ (II) Upgrading Project of a Meat Processing Factory in Singapore​ The factory's original temperature and humidity control system was outdated, unable to precisely control the temperature in the cold storage area, resulting in thawing and refreezing of some meat products, which affected the meat quality and shelf life. In addition, the drainage system had problems such as insufficient pipe slope and the lack of filtration devices at drainage outlets, leading to poor sewage discharge and frequent water accumulation on the workshop floor.​ After upgrading according to the SS 585:2017 standard, an intelligent temperature and humidity control system was installed, which can monitor and adjust temperature and humidity in real - time. The drainage pipes were re - laid to ensure that the slope met the standard, and filters and P - traps were added at the drainage outlets. After the renovation, the microbial over - standard rate of products decreased from 8% before the renovation to 1.2%, production efficiency increased by 15%, and product losses caused by temperature and humidity problems were reduced by 20%. Both economic benefits and food safety levels were significantly improved.​ III. Guangzhou Cleanroom Construction Co., Ltd.: A Deep Practitioner of the SS 585:2017 Standard​ (I) Air Purification Solutions​ The high - efficiency air purification equipment developed by Guangzhou Cleanroom Construction Co., Ltd. uses H13 - grade high - efficiency filters, with a filtration efficiency of 99.99% for particles of 0.3μm, stably ensuring that the air cleanliness of the workshop reaches ISO Class 8 or even higher standards. Meanwhile, the company has a professional air flow organization design team that can design the most reasonable air supply and return schemes according to the workshop layout and production requirements. For example, in large - scale food processing workshops, the air flow organization form of top - side supply and double - side bottom - return is adopted, effectively avoiding air flow dead corners and ensuring the uniform distribution of clean air.​ (II) Temperature and Humidity Control System​ The company's temperature and humidity control system has high - precision regulation capabilities, with a temperature control accuracy of ± 0.5°C and a humidity control accuracy of ± 3%. It can customize personalized solutions according to different food production needs. For example, the temperature and humidity control system designed for chocolate production workshops can stably control the workshop temperature at 18 - 22°C and humidity at 40% - 50% in high - temperature summer environments, preventing chocolate from melting and frosting on the surface and ensuring product quality. ​ (III) Overall Planning and Services​ In addition to supplying core equipment, Guangzhou Cleanroom Construction Co., Ltd. also provides one - stop services covering pre - construction planning and design, equipment installation and commissioning, and after - sales maintenance. In the planning and design stage, the company's team will thoroughly understand the production processes, product types, and other information of food enterprises, and conduct scientific and reasonable workshop layout planning in combination with the SS 585:2017 standard, including functional area division, design of pedestrian and logistics channels, and layout of ventilation and drainage systems. During the installation and commissioning process, every link is strictly controlled to ensure stable equipment operation and that all indicators meet the standard requirements. In terms of after - sales maintenance, regular inspection services are provided to promptly detect and solve problems that occur during equipment operation, ensuring the continuous compliant production of food factories. With years of industry experience and a professional technical team, the company has successfully assisted more than 50 food enterprises in completing factory upgrading and renovation projects, receiving unanimous praise from customers.​ Adhering to Singapore Standard SS 585:2017 Design Standards for Food Factories is the key for food enterprises to achieve safe production and enhance their market competitiveness. Guangzhou Cleanroom Construction Co., Ltd. is willing to join hands with food enterprises with its professional capabilities to jointly create food production environments that meet high standards, safeguard the food safety defense line, and contribute to the healthy development of the food industry.  
2025-06-24
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Latest company case about Custom Cleanroom Booth Experts for Electronics Factories, Quality Assurance from the Source Manufacturer

Custom Cleanroom Booth Experts for Electronics Factories, Quality Assurance from the Source Manufacturer

In the field of electronics manufacturing, even a single speck of dust can be a “fatal killer” to precision components. From chip manufacturing to precision assembly, every step demands an extremely stringent clean environment. Guangzhou Cleanroom Construction Co., Ltd., as a source manufacturer with years of experience in the purification equipment industry, offers professional custom cleanroom booth solutions, creating a dust-free and worry-free production space for electronics factories.​ I. Source Manufacturer: No Middleman Markup​ Unlike trading companies and distributors, Guangzhou Cleanroom Construction Co., Ltd. owns its own production factory. Every aspect, from research and development, raw material procurement, to production and quality inspection, is strictly controlled by our in-house team. Without the multiple markups from middlemen, we can offer the greatest price advantages to our customers, enabling electronics factories to obtain high-quality cleanroom booths at a more economical cost. Moreover, as a source manufacturer, we can respond more quickly to customer needs. From communicating custom solutions to product delivery and installation, the entire process is carried out efficiently, significantly shortening the project cycle. II. Tailor-Made Solutions: Meeting the Diverse Needs of Electronics Factories​ The production processes in electronics factories vary greatly, leading to different requirements for cleanroom booths. Cleanroom Construction understands this well. Our professional team will conduct on-site visits to electronics factories, thoroughly understand key information such as production processes, equipment layout, and cleanliness requirements, and customize cleanroom booths according to actual needs. Whether it’s a small local purification area or a large workshop-level clean space; whether there are special requirements for temperature, humidity, wind speed, or specific fireproof and anti-static standards need to be met, we can provide the most suitable solutions. Every detail, from the design of the booth structure and the selection of high-efficiency filters, to the lighting system and air flow organization planning, is carefully considered to ensure that the cleanroom booth perfectly matches the production of electronics factories.​ III. Advanced Technology: Ensuring Cleanliness Quality​ As a professional manufacturer in the industry, Guangzhou Cleanroom Construction Co., Ltd. is equipped with advanced production equipment and mature production processes. We use high-quality materials to manufacture cleanroom booths. The frame is made of high-strength aluminum alloy or stainless steel, which is lightweight, strong, and corrosion-resistant; the enclosure structure uses high-quality sandwich panels, which have excellent thermal insulation, sound insulation, and sealing properties. In terms of air purification technology, our cleanroom booths are equipped with high-efficiency filters that can effectively filter dust particles larger than 0.3 microns, easily achieving cleanliness levels from ISO 4 to ISO 8, meeting the strict requirements of different electronics production processes for clean environments. At the same time, through scientific air flow organization design, we ensure uniform air flow within the cleanroom booth, avoiding eddies and dead corners, and maintaining a stable clean environment. ​ IV. One-Stop Service: Worry-Free After-Sales Support​ From project consultation, solution design, to production, installation, debugging, and maintenance, Cleanroom Construction provides one-stop services. Our installation team is highly experienced and can quickly and standardly complete the construction of cleanroom booths, minimizing the impact on the normal production of electronics factories. After project delivery, we also provide comprehensive after-sales support, regularly visiting customers to check the operation status of cleanroom booths; if any problems arise, our after-sales team will respond and resolve them in the shortest possible time, allowing electronics factories to focus on production operations without worries.​ Choosing Guangzhou Cleanroom Construction Co., Ltd. means choosing the quality and guarantee of a source manufacturer, as well as professional custom cleanroom booth solutions. We manufacture products with ingenuity and serve customers with sincerity, helping electronics factories produce higher-quality electronic products in a clean environment and moving towards a broader market. We look forward to working with you to create a clean future for electronics manufacturing!  
2025-06-24
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Latest company case about Hospital Central Supply Room Stainless Steel Platform Stand Design (1200×550×200mm)

Hospital Central Supply Room Stainless Steel Platform Stand Design (1200×550×200mm)

Application Background This stainless steel platform stand is designed for hospital central supply rooms, providing a sterile, durable, and easy-to-clean support solution for medical equipment, sterilization trays, and instrument storage. Its corrosion-resistant structure meets the strict hygiene requirements of medical environments. Design Specifications 1. Dimensions & Structure Overall size: 1200mm (L) × 550mm (W) × 200mm (H) Optimized for sterilization carts, instrument trays, and medical device placement Low-profile design (200mm height) ensures stability while allowing easy access Frame material: 38×38×1.0304 stainless steel square tube High strength & rigidity to support heavy medical equipment Smooth, non-porous surface prevents bacterial accumulation Resistant to chemicals, moisture, and high-temperature sterilization 2. Adjustable Feet (4 Units) Stainless steel or nylon adjustable feet for stability on uneven floors Anti-slip & vibration-damping to prevent equipment movement Easy height adjustment for leveling on hospital flooring Key Advantages for Medical Use ✔ Hygienic Design – Easy to disinfect with hospital-grade cleaners; no rust or corrosion✔ Heavy-Duty Load Capacity – Supports sterilization containers, surgical instrument trays, and medical devices✔ Smooth, Seamless Welding – No crevices for bacteria or contaminants to accumulate✔ Mobility-Friendly – Compatible with medical carts and trolleys when needed Customization Options Electropolished or antimicrobial-coated finishes Additional support bars for heavier loads Locking casters (optional) for mobile use This medical-grade stainless steel platform stand is an ideal solution for central sterile supply departments (CSSD), operating rooms, and laboratory settings. For specialized hospital requirements, contact us for tailored solutions. Contact us for quotes, technical drawings, and customization!    
2025-06-24
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