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China Guangzhou Cleanroom Construction Co., Ltd.
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Guangzhou Cleanroom Construction Co., Ltd.
Establishment & Vision: Guangzhou Cleanroom Construction Co., Ltd. was founded in 2010 and is committed to becoming a one-stop cleanroom construction and solutions partner for customers, contributing to the development of the global cleanroom industry. ​Qualifications and Honors: It is a high-quality enterprise in China's cleanroom system engineering and equipment manufacturing industry, and has been recognized as a high-tech enterprise and a "little giant" of technological innovation in Guangzhou, demonstrating its leading position in the industry. Base Locations: The company has a rational layout, with its production base located in Panyu, Guangzhou, and its sales center in Pazhou, Guangzhou. The two locations operate in coordination, ensuring efficient production of products and quick response to market demands, providing convenient services to customers. We warmly welcome customers from home and abroad to visit us. Localized Services: In the process of global development, the company attaches great importance to localized services and has established stable partnerships in many countries such as Indonesia, Saudi Arabia, and the Philippines. This layout ensures that we can provide local customers with timely on-site responses, tailored solutions, and efficient after-sales services, allowing customers to experience seamless support. Certifications and Patents: The company has passed multiple international certifications such as ISO 9001, ISO 14001, and ISO 45001, and owns numerous utility model patents and design patents, reflecting its strict quality management and strong research and development capabilities. It is also a member of many professional associations such as the Guangdong Laboratory Association and the Shanghai Laboratory Equipment Association, and actively participates in well-known industry exhibitions such as the National Hospital Construction Conference and the Munich Shanghai Analysis & Biochemistry Exhibition, always keeping pace with the industry frontier. Product Applications: The company focuses on providing comprehensive solutions for laboratory and medical cleanroom construction. Its products include air showers, pass boxes, workbenches, dissection tables, fume hoods, etc., which are widely used in various fields such as animal experiments, biosafety, food safety, chemical industry, semiconductors, healthcare, and pharmaceuticals. Customer Cases: With high-quality products and services, it has won the trust of many well-known institutions such as Nanshan Pharmaceutical, Sun Yat-sen University, Tsinghua University, Hong Kong University of Science and Technology, Guangdong Medical Device Quality Supervision and Inspection Institute, and Shenzhen CDC.
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GCC Celebrates 15th Anniversary and New Factory Relocation 2025-11-12 In 2025, Guangzhou Cleanroom Construction Co., Ltd. (GCC) proudly celebrates its 15th anniversary and factory relocation. The new facility is located in Panyu District, Guangzhou, China. It marks an important milestone in GCC’s continuous growth and innovation journey. 15 Years of Excellence in Cleanroom Engineering Since 2010, GCC has focused on cleanroom design, manufacturing, and installation. The company serves pharmaceutical, electronics, healthcare, and research industries. Over the years, GCC has built a strong reputation for quality and reliability. Its core products include: Grossing Stations Fume Hoods Biosafety Cabinets Laminar Flow Cabinets Moreover, GCC combines advanced engineering with strict quality control. As a result, it has gained trust from customers both in China and abroad. A Modern Facility for a Smarter Future The new three-story factory integrates production, R&D, quality control, and logistics. It also houses administration offices in one modern complex. Each section is carefully designed to improve efficiency and product quality. In addition, the factory features automated production lines and precision testing instruments. Therefore, every stage of manufacturing follows high standards of safety and accuracy. “The relocation marks a new chapter for GCC. We will continue to focus on professionalism, innovation, and global collaboration.” — GCC Management Team Driving Innovation and Global Collaboration GCC always upholds its three core values: Quality, Innovation, and Customer Focus. The company aims to expand its OEM and ODM capabilities. It also plans to strengthen international partnerships and promote sustainable development. Furthermore, GCC continues to explore intelligent manufacturing technologies. With its new facility, the company is better positioned to deliver high-quality solutions worldwide. Contact Information Address: Panyu District, Guangzhou, China Email: sales01@gzkunling.com Phone: +86 133 1627 2505 WhatsApp: +86 181 4863 5992 Conclusion As GCC celebrates 15 years of excellence, it expresses deep gratitude to all clients and partners. The new factory opens a new chapter for growth and innovation. Going forward, GCC is committed to building a cleaner, smarter, and more sustainable future for laboratories worldwide.
Semiconductor and Electronics Industry Cleanroom Solutions 2025-07-31 Unique Requirements and Standards​ Extreme cleanliness demands: Dominated by ISO 5-7 grades (Class 100-10,000), with advanced packaging areas requiring ISO 4 (Class 10) to control particles ≥0.1μm.​ Multidimensional control: Simultaneously manage temperature (20-24℃±0.1℃), humidity (40-50%±2%), vibration (≤50μm/s), and static electricity (≤100V).​ International standards: Must comply with SEMI S2, ISO 14644, and GMP for electronics, with strict process isolation requirements between different production stages.​ Core Solutions​ Air Purification System​ Filtration hierarchy: Pre-filter (G4) + medium-efficiency filter (F9) + sub-high efficiency filter (H13) + terminal ULPA filter (99.999% efficiency for ≥0.12μm particles).​ Airflow design: Full coverage unidirectional flow (0.45m/s±20%) in core areas, with air change rates up to 500 times/hour.​ Pressure control: Gradient pressure difference (≥5Pa between adjacent zones) to prevent cross-contamination.​ Contamination Control Measures​ Material management: Airlocks for incoming materials, dedicated unpacking and cleaning procedures, and ultra-pure water (18.2MΩ·cm) with TOC ≤10ppb.​ Surface treatment: Welded stainless steel walls (304/316L), seamless PVC floors, and silicone-free sealants.​ Chemical control: Local exhaust systems for etching processes, with acid gas removal efficiency ≥99%.​ Lean Operation Strategies​ Intelligent monitoring: Real-time particle counters, temperature/humidity sensors, and IoT-based centralized control systems.​ Energy optimization: Heat recovery units (energy saving ≥30%), variable frequency fans, and LED cleanroom lighting.​ Maintenance protocols: Quarterly HEPA/ULPA filter integrity testing, monthly airflow velocity verification, and annual comprehensive performance validation.​ Future Trends​ Miniaturization: Development towards ISO 3 (Class 1) cleanrooms to adapt to 3nm and smaller process nodes.​ Green innovation: Adoption of low-VOC materials and renewable energy integration.​ Digital transformation: AI-driven predictive maintenance and digital twins for virtual commissioning.​ Semiconductor cleanrooms require a balance of extreme cleanliness, process stability, and operational efficiency. By integrating advanced filtration technology, precise environmental control, and intelligent management systems, these critical facilities support the production of high-performance electronic components.
Pharmaceutical Cleanroom Solutions 2025-07-31 Unique Requirements and Standards​ Strict classification: Divided into Grade A/B/C/D according to GMP. Grade A (ISO 5) is used for sterile preparation filling, while Grade D (ISO 8) is suitable for non-sterile API production.​ Multi-parameter control: Temperature 18-26℃, humidity 45-65%, unidirectional airflow velocity in Grade A areas 0.36-0.54m/s, pressure differential gradient ≥10Pa.​ Compliance requirements: Must meet WHO GMP, FDA cGMP and China GMP. Regular environmental monitoring (viable airborne particles, settleable bacteria, surface microorganisms) is required.​ Core Solutions​ Air Purification System​ Filtration system: Three-stage filtration of primary (G4) + medium (F8) + high efficiency (H14) filters. Grade A areas adopt 100% fresh air with full exhaust.​ Airflow organization: Grade A areas are fully covered with HEPA filters. Grade B areas use non-unidirectional airflow with air change rate ≥20 times/hour.​ Disinfection system: Integrated VHP (vaporized hydrogen peroxide) sterilization, with qualified biological indicator challenge (spore kill rate ≥6 log).​ Contamination Prevention Measures​ Personnel management: Dedicated gowning process (first change → second change → air lock). Grade A areas require sterile coveralls + breathing masks.​ Material control: Raw materials enter through sterile pass-through boxes. Primary packaging materials need online sterilization (dry heat/moist heat).​ Equipment design: Surfaces in contact with pharmaceuticals use 316L stainless steel, with welded and polished Ra ≤0.8μm, no dead corners.​ Lean Operation Strategies​ Real-time monitoring: Online particle counters (recording every 30 minutes), continuous temperature and humidity tracking, automatic alarm for exceeding standards.​ Energy-saving solutions: Adopt variable frequency air handling units + heat recovery devices, and reduce frequency during non-production periods (energy saving ≥25%).​ Maintenance plan: HEPA filter leak detection annually, quarterly verification of air conditioning systems, full-item testing of process water weekly.​ Future Trends​ Modular construction: Prefabricated cleanroom components, installation cycle shortened by 40%, meeting flexible production needs.​ Digital upgrading: Environmental data traceability based on MES system, AI predicts filter lifespan.​ Green certification: Use low-carbon materials, reuse wastewater/waste gas after reaching standards, reduce environmental load.​ Pharmaceutical cleanrooms need to balance sterility assurance and production efficiency. Through strict hierarchical management, advanced purification technology and intelligent operation, they provide a core barrier for pharmaceutical quality.​ Pharmaceutical Cleanrooms & GMP Basics Questions 1.What is a Pharmaceutical Clean Room? 2.What is a Clean Area in the Pharmaceutical Industry? 3.What is a Clean Room in GMP? 4.What is a Clean Room in a Pharmacy? Cleanroom Standards & Classifications 5.What are the Cleanroom Standards for Pharmaceuticals? 6.What is the FDA cGMP for Pharmaceuticals? Cleanroom Equipment & Applications 7.What is a Downflow Booth in the Pharmaceutical Industry? 8.What is the Role of Clean Room Panels in the Pharmaceutical Industry? Importance of Cleanrooms in Pharma 9.Why are Clean Rooms Important in the Pharmaceutical Industry? GMP & cGMP in Pharmaceuticals 10.What is GMP and cGMP in Pharma? For further inquiries, please consult the sales team.
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102, Building 4, No. 23 Yongfeng Road, Yongshan Village, Shiqi Town, Panyu District, Guangzhou City, Guangdong Province
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