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— ABOUT US —

Providing the best air clean solution for each field on the world

AIRTECH

Suzhou Antai Airtech Co., Ltd

SUZHOU ANTAI AIRTECH CO.,LTD(SAT) is a joint venture organized by JIANGSU SUZHOU PURIFICATION EQUIPMENT(GROUP) INCORPORATION(SPEG) and AIRTECH JAPAN,LTD(ATJ).Continuing as the leader in product technology, it's the combination of scientific research, development, production and sales with independent research institute and laborites, which makes SAT the best clean air solution.

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— NEWS —

To know the latest technology, product and information of SAT.

Sujing Antai Holds Comprehensive Emergency Drill

To strengthen employees’ fire safety awareness, improve their response capacity in emergencies, and help them master proper fire extinguisher operation and evacuation skills, Sujing Antai organized a full-staff fire safety practical drill on May 14. Pre-drill Briefing & Fire Extinguisher Tutorial At 4 p.m., all staff gathered at the factory compound. First, General Manager Lu delivered a pre-drill mobilization speech, stressing that fire safety relies on prevention. Minister Fu, Chief Safety Commander, explained fire safety knowledge and demonstrated how to use fire extinguishers. General Manager Lu then officially announced the launch of the 2026 Annual Fire Emergency Drill. Under the guidance of Chief Safety Commander Minister Yao, each team activated the fire emergency response plan, carrying out alarm triggering, site cordoning, personnel evacuation and fire suppression procedures in an orderly manner. Live Fire Extinguishing Practice The live fire-fighting session followed. Four fire buckets were ignited, and employees stepped forward enthusiastically to put out the flames with fire extinguishers on site amid billowing smoke. In a positive and collaborative atmosphere, all staff mastered fire extinguisher operation and gained deeper understanding of fire safety priorities. Closing Summary Finally, Chairman Jin delivered closing remarks and comments on the drill. He highlighted the great significance of regular fire drills: this activity has further raised employees’ awareness of fire hazard prevention and their self-rescue capabilities during emergencies. It accumulated practical experience for on-site emergency response and verified the feasibility of the company’s fire emergency plan, laying a solid foundation for the company’s future fire safety management work.

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To strengthen employees’ fire safety awareness, improve their response capacity in emergencies, and help them master proper fire extinguisher operation and evacuation skills, Sujing Antai organized a full-staff fire safety practical drill on May 14. Pre-drill Briefing & Fire Extinguisher Tutorial At 4 p.m., all staff gathered at the factory compound. First, General Manager Lu delivered a pre-drill mobilization speech, stressing that fire safety relies on prevention. Minister Fu, Chief Safety Commander, explained fire safety knowledge and demonstrated how to use fire extinguishers. General Manager Lu then officially announced the launch of the 2026 Annual Fire Emergency Drill. Under the guidance of Chief Safety Commander Minister Yao, each team activated the fire emergency response plan, carrying out alarm triggering, site cordoning, personnel evacuation and fire suppression procedures in an orderly manner. Live Fire Extinguishing Practice The live fire-fighting session followed. Four fire buckets were ignited, and employees stepped forward enthusiastically to put out the flames with fire extinguishers on site amid billowing smoke. In a positive and collaborative atmosphere, all staff mastered fire extinguisher operation and gained deeper understanding of fire safety priorities. Closing Summary Finally, Chairman Jin delivered closing remarks and comments on the drill. He highlighted the great significance of regular fire drills: this activity has further raised employees’ awareness of fire hazard prevention and their self-rescue capabilities during emergencies. It accumulated practical experience for on-site emergency response and verified the feasibility of the company’s fire emergency plan, laying a solid foundation for the company’s future fire safety management work.

Product Application | How Is an IV Infusion Bag Prepared?

As winter arrives with plummeting temperatures, people easily catch colds. For severe cases where oral medicine fails to work, doctors will recommend intravenous infusion therapy, commonly known as IV drip. So how exactly is an IV drip bag compounded? I. What Is a Pharmacy Intravenous Admixture Service (PIVAS)? 1. Definition of PIVAS Traditionally, intravenous infusions were prepared by nurses in treatment rooms. In modern hospitals, the Pharmacy Intravenous Admixture Service (PIVAS) has been established to improve the quality of finished IV infusions, ensure safe, effective, economical and appropriate clinical intravenous medication, and free nurses from tedious daily compounding work so they can devote more time to direct patient care. Simply put, PIVAS centralizes the preparation and distribution of intravenous medications. Under physicians’ prescriptions or medication orders, pharmacy professionals first conduct clinical suitability reviews. Then pharmaceutical technical staff perform aseptic mixing and compounding of intravenous drugs in clean environments following strict sterile operation standards, producing finished infusions ready for direct clinical intravenous administration. 2. Advantages of Centralized Intravenous Medication Compounding First, standardized compounding safeguards drug quality and infusion safety. Supported by rigorous preparation workflows and quality control systems, PIVAS minimizes risks of drug contamination and incompatible drug combinations, guaranteeing the safety and efficacy of all infusions. Second, it streamlines pharmaceutical inventory management and reduces drug waste. It also relieves nurses of heavy compounding workloads to enhance the quality of clinical nursing care. Meanwhile, pharmacists fully leverage their professional expertise through multi-step processes including prescription review, dispensing and double-checking. Third, PIVAS elevates occupational protection. Cytotoxic and other hazardous drugs are compounded under negative pressure, drastically lowering toxic exposure risks for medical staff and patients. PIVAS also creates a platform for pharmacists to participate in rational clinical medication, advancing the development of clinical pharmacy. II. The Full Workflow of Preparing an IV Infusion Bag 1. PIVAS Layout & Medication Compounding Process PIVAS is a relatively enclosed space with stringent cleanliness requirements, divided into three functional zones: clean area, controlled non-clean area and auxiliary service area. The compounding room meets Class 10,000 cleanliness standards, with horizontal laminar flow clean benches and biosafety cabinets as standard air purification equipment for all PIVAS facilities. The full compounding workflow consists of six core steps: 1. Medication Order Review: Pharmacists assess the rationality of each prescription, arrange medication administration sequences and print infusion labels. 2. Labeling, Dispensing & Cross-Verification: Infusion bags are labeled, and corresponding drugs are sorted out per label. Double-person verification is mandatory at every stage; batches can only enter designated compounding rooms after full confirmation. 3. Aseptic Mixing & Compounding: In dedicated compounding rooms, pharmacists conduct sterile drug mixing on horizontal laminar flow benches or biosafety cabinets to produce finished IV infusions. 4. Finished Product Inspection: Pharmacists recheck the quality of completed infusions and authorize release for clinical use. 5. Sorting & Packaging: Qualified IV bags are sorted by ward, sealed in locked packaging and delivered to clinical departments for patients. 2. How AIRTECH Supports the Development of PIVAS Suzhou AIRTECH Air Technology Co., Ltd. integrates R&D, manufacturing and sales, delivering comprehensive air purification solutions for all sectors. For decades, we have provided reliable services to medical institutions, drug regulatory authorities and drug testing laboratories, and supplied biosafety cabinets and clean benches for key national projects. Our products also played a vital role in combating the SARS and COVID-19 outbreaks. As early as 1998, AIRTECH partnered with leading IV infusion manufacturers to supply matching biosafety cabinets and clean benches, earning widespread recognition from industrial partners and hospitals and laying the foundation for domestic PIVAS development. Over decades, we have maintained long-term cooperation with major large-volume infusion enterprises and engineering companies, supplying products and services to more than 200 hospital PIVAS nationwide with consistent positive feedback. AIRTECH’s specially customized Class II biosafety cabinets and horizontal laminar flow clean benches for PIVAS deliver ISO Class 5 (Class 100) or higher sterile operation environments in compounding zones, while featuring easy cleaning and disinfection. Optional acce

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As winter arrives with plummeting temperatures, people easily catch colds. For severe cases where oral medicine fails to work, doctors will recommend intravenous infusion therapy, commonly known as IV drip. So how exactly is an IV drip bag compounded? I. What Is a Pharmacy Intravenous Admixture Service (PIVAS)? 1. Definition of PIVAS Traditionally, intravenous infusions were prepared by nurses in treatment rooms. In modern hospitals, the Pharmacy Intravenous Admixture Service (PIVAS) has been established to improve the quality of finished IV infusions, ensure safe, effective, economical and appropriate clinical intravenous medication, and free nurses from tedious daily compounding work so they can devote more time to direct patient care. Simply put, PIVAS centralizes the preparation and distribution of intravenous medications. Under physicians’ prescriptions or medication orders, pharmacy professionals first conduct clinical suitability reviews. Then pharmaceutical technical staff perform aseptic mixing and compounding of intravenous drugs in clean environments following strict sterile operation standards, producing finished infusions ready for direct clinical intravenous administration. 2. Advantages of Centralized Intravenous Medication Compounding First, standardized compounding safeguards drug quality and infusion safety. Supported by rigorous preparation workflows and quality control systems, PIVAS minimizes risks of drug contamination and incompatible drug combinations, guaranteeing the safety and efficacy of all infusions. Second, it streamlines pharmaceutical inventory management and reduces drug waste. It also relieves nurses of heavy compounding workloads to enhance the quality of clinical nursing care. Meanwhile, pharmacists fully leverage their professional expertise through multi-step processes including prescription review, dispensing and double-checking. Third, PIVAS elevates occupational protection. Cytotoxic and other hazardous drugs are compounded under negative pressure, drastically lowering toxic exposure risks for medical staff and patients. PIVAS also creates a platform for pharmacists to participate in rational clinical medication, advancing the development of clinical pharmacy. II. The Full Workflow of Preparing an IV Infusion Bag 1. PIVAS Layout & Medication Compounding Process PIVAS is a relatively enclosed space with stringent cleanliness requirements, divided into three functional zones: clean area, controlled non-clean area and auxiliary service area. The compounding room meets Class 10,000 cleanliness standards, with horizontal laminar flow clean benches and biosafety cabinets as standard air purification equipment for all PIVAS facilities. The full compounding workflow consists of six core steps: 1. Medication Order Review: Pharmacists assess the rationality of each prescription, arrange medication administration sequences and print infusion labels. 2. Labeling, Dispensing & Cross-Verification: Infusion bags are labeled, and corresponding drugs are sorted out per label. Double-person verification is mandatory at every stage; batches can only enter designated compounding rooms after full confirmation. 3. Aseptic Mixing & Compounding: In dedicated compounding rooms, pharmacists conduct sterile drug mixing on horizontal laminar flow benches or biosafety cabinets to produce finished IV infusions. 4. Finished Product Inspection: Pharmacists recheck the quality of completed infusions and authorize release for clinical use. 5. Sorting & Packaging: Qualified IV bags are sorted by ward, sealed in locked packaging and delivered to clinical departments for patients. 2. How AIRTECH Supports the Development of PIVAS Suzhou AIRTECH Air Technology Co., Ltd. integrates R&D, manufacturing and sales, delivering comprehensive air purification solutions for all sectors. For decades, we have provided reliable services to medical institutions, drug regulatory authorities and drug testing laboratories, and supplied biosafety cabinets and clean benches for key national projects. Our products also played a vital role in combating the SARS and COVID-19 outbreaks. As early as 1998, AIRTECH partnered with leading IV infusion manufacturers to supply matching biosafety cabinets and clean benches, earning widespread recognition from industrial partners and hospitals and laying the foundation for domestic PIVAS development. Over decades, we have maintained long-term cooperation with major large-volume infusion enterprises and engineering companies, supplying products and services to more than 200 hospital PIVAS nationwide with consistent positive feedback. AIRTECH’s specially customized Class II biosafety cabinets and horizontal laminar flow clean benches for PIVAS deliver ISO Class 5 (Class 100) or higher sterile operation environments in compounding zones, while featuring easy cleaning and disinfection. Optional acce

Product Application | Safeguard Sample Integrity, Accelerate Commercialization of Scientific and Technological Achievements

The commercialization of scientific and technological achievements has become a hot topic in recent years. What exactly does it mean? How is it implemented? And what is its connection to the air purification industry? This article will elaborate on these questions. I. What Is the Commercialization of Scientific and Technological Achievements? 1. Significance of Commercializing Scientific and Technological Achievements As stipulated in Article 2 of the newly revised Law of the People's Republic of China on Promoting the Transformation of Scientific and Technological Achievements (2015), scientific and technological achievements refer to practically valuable outputs generated through scientific research and technological development. Service-related scientific and technological achievements are those completed to fulfill work tasks assigned by research institutes, universities, enterprises and other entities, or developed mainly by utilizing the material and technical resources of such entities. There are six primary modes for commercializing scientific and technological achievements: 1. Self-investment for independent transformation; 2. Transfer of scientific and technological achievements to other parties; 3. Licensing other parties to utilize scientific and technological achievements; 4. Joint transformation with other parties by taking scientific and technological achievements as cooperation conditions; 5. Capital contribution by valuing scientific and technological achievements for equity or investment ratio conversion; 6. Other forms agreed through negotiation. To fully understand the commercialization of scientific and technological achievements, four core points should be clarified: First, its core objective is to boost productivity; Second, its target scope is limited to practically valuable scientific and technological achievements, not all research outputs; Third, it covers standardized, systematic transformation workflows; Fourth, it delivers tangible economic and industrial outcomes. II. How to Boost the Commercialization of Scientific and Technological Achievements 1. AIRTECH Empowers the Transformation of Scientific and Technological Achievements Suzhou AIRTECH Air Technology Co., Ltd. delivers comprehensive integrated air purification solutions for diverse industries. Our flagship products including biosafety cabinets and clean benches are widely deployed in scientific research and education sectors, making substantial contributions to facilitating lab research, accelerating achievement commercialization and advancing industrial upgrading. Over the years, numerous prestigious universities and research institutions nationwide have achieved remarkable progress in translating research results into real-world applications. A well-controlled laboratory environment is an indispensable prerequisite for researchers. AIRTECH biosafety cabinets deliver robust safety protection for experimental spaces, while their stable performance and intelligent design greatly improve research efficiency. Additionally, clean benches serve as fundamental lab equipment. They generate localized sterile working zones via laminar air circulation and high-efficiency filtration, classified into horizontal laminar flow and vertical laminar flow types based on airflow patterns. Renowned for consistent reliable quality, AIRTECH clean benches are the top choice for clients, powering the full-cycle transformation of scientific achievements. III. Why Choose AIRTECH ? 1. Core Advantages of AIRTECH Biosafety Cabinets AIRTECH biosafety cabinets support configurable HEPA/ULPA filters tailored to user demands. Adopting seamless closed-cell sealing made of polymer self-flow shaping material and a specially optimized air supply structure, the cabinets maximize air outlet coverage to maintain premium experimental conditions and lay a solid foundation for high-quality research outputs. Equipped with a large-format color touchscreen, the cabinets feature intuitive, user-friendly operation for quick mastery by teachers and students. The screen displays real-time key operational parameters such as airflow velocity and filter service status, integrated with an intelligent monitoring system that triggers audible and visual alarms for all malfunctions, enabling full traceability of lab safety records. In terms of safety protection: The double-layer negative pressure enclosure, paired with our proprietary unobstructed air return and leakage-blocking technologies, effectively prevents the spread of hazardous contaminants. For easy sanitization, the entire working chamber is integrally molded from SUS304 stainless steel, and the full-size front window allows dead-spot-free cleaning to curb bacterial proliferation. Ergonomic & Humanized Design: • 10° inclined front panel for comfortable viewing; exclusive sliding window positioning lift system; wide curved hand rest; h

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The commercialization of scientific and technological achievements has become a hot topic in recent years. What exactly does it mean? How is it implemented? And what is its connection to the air purification industry? This article will elaborate on these questions. I. What Is the Commercialization of Scientific and Technological Achievements? 1. Significance of Commercializing Scientific and Technological Achievements As stipulated in Article 2 of the newly revised Law of the People's Republic of China on Promoting the Transformation of Scientific and Technological Achievements (2015), scientific and technological achievements refer to practically valuable outputs generated through scientific research and technological development. Service-related scientific and technological achievements are those completed to fulfill work tasks assigned by research institutes, universities, enterprises and other entities, or developed mainly by utilizing the material and technical resources of such entities. There are six primary modes for commercializing scientific and technological achievements: 1. Self-investment for independent transformation; 2. Transfer of scientific and technological achievements to other parties; 3. Licensing other parties to utilize scientific and technological achievements; 4. Joint transformation with other parties by taking scientific and technological achievements as cooperation conditions; 5. Capital contribution by valuing scientific and technological achievements for equity or investment ratio conversion; 6. Other forms agreed through negotiation. To fully understand the commercialization of scientific and technological achievements, four core points should be clarified: First, its core objective is to boost productivity; Second, its target scope is limited to practically valuable scientific and technological achievements, not all research outputs; Third, it covers standardized, systematic transformation workflows; Fourth, it delivers tangible economic and industrial outcomes. II. How to Boost the Commercialization of Scientific and Technological Achievements 1. AIRTECH Empowers the Transformation of Scientific and Technological Achievements Suzhou AIRTECH Air Technology Co., Ltd. delivers comprehensive integrated air purification solutions for diverse industries. Our flagship products including biosafety cabinets and clean benches are widely deployed in scientific research and education sectors, making substantial contributions to facilitating lab research, accelerating achievement commercialization and advancing industrial upgrading. Over the years, numerous prestigious universities and research institutions nationwide have achieved remarkable progress in translating research results into real-world applications. A well-controlled laboratory environment is an indispensable prerequisite for researchers. AIRTECH biosafety cabinets deliver robust safety protection for experimental spaces, while their stable performance and intelligent design greatly improve research efficiency. Additionally, clean benches serve as fundamental lab equipment. They generate localized sterile working zones via laminar air circulation and high-efficiency filtration, classified into horizontal laminar flow and vertical laminar flow types based on airflow patterns. Renowned for consistent reliable quality, AIRTECH clean benches are the top choice for clients, powering the full-cycle transformation of scientific achievements. III. Why Choose AIRTECH ? 1. Core Advantages of AIRTECH Biosafety Cabinets AIRTECH biosafety cabinets support configurable HEPA/ULPA filters tailored to user demands. Adopting seamless closed-cell sealing made of polymer self-flow shaping material and a specially optimized air supply structure, the cabinets maximize air outlet coverage to maintain premium experimental conditions and lay a solid foundation for high-quality research outputs. Equipped with a large-format color touchscreen, the cabinets feature intuitive, user-friendly operation for quick mastery by teachers and students. The screen displays real-time key operational parameters such as airflow velocity and filter service status, integrated with an intelligent monitoring system that triggers audible and visual alarms for all malfunctions, enabling full traceability of lab safety records. In terms of safety protection: The double-layer negative pressure enclosure, paired with our proprietary unobstructed air return and leakage-blocking technologies, effectively prevents the spread of hazardous contaminants. For easy sanitization, the entire working chamber is integrally molded from SUS304 stainless steel, and the full-size front window allows dead-spot-free cleaning to curb bacterial proliferation. Ergonomic & Humanized Design: • 10° inclined front panel for comfortable viewing; exclusive sliding window positioning lift system; wide curved hand rest; h

Sujing Antai Holds Comprehensive Emergency Drill 2026-05-15

To strengthen employees’ fire safety awareness, improve their response capacity in emergencies, and help them master proper fire extinguisher operation and evacuation skills, Sujing Antai organized a full-staff fire safety practical drill on May 14. Pre-drill Briefing & Fire Extinguisher Tutorial At 4 p.m., all staff gathered at the factory compound. First, General Manager Lu delivered a pre-drill mobilization speech, stressing that fire safety relies on prevention. Minister Fu, Chief Safety Commander, explained fire safety knowledge and demonstrated how to use fire extinguishers. General Manager Lu then officially announced the launch of the 2026 Annual Fire Emergency Drill. Under the guidance of Chief Safety Commander Minister Yao, each team activated the fire emergency response plan, carrying out alarm triggering, site cordoning, personnel evacuation and fire suppression procedures in an orderly manner. Live Fire Extinguishing Practice The live fire-fighting session followed. Four fire buckets were ignited, and employees stepped forward enthusiastically to put out the flames with fire extinguishers on site amid billowing smoke. In a positive and collaborative atmosphere, all staff mastered fire extinguisher operation and gained deeper understanding of fire safety priorities. Closing Summary Finally, Chairman Jin delivered closing remarks and comments on the drill. He highlighted the great significance of regular fire drills: this activity has further raised employees’ awareness of fire hazard prevention and their self-rescue capabilities during emergencies. It accumulated practical experience for on-site emergency response and verified the feasibility of the company’s fire emergency plan, laying a solid foundation for the company’s future fire safety management work.
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