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.  

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

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

Give me a leaf, and I can grow an entire forest. Much like Sun Wukong in Journey to the West, who plucks a single hair to conjure hundreds of monkeys—this seemingly magical feat is entirely achievable. That’s exactly what we’ll cover today: plant tissue culture technology.   I. What Is Plant Tissue Culture and a Tissue Culture Laboratory?   1. Definition of Plant Tissue Culture   Plant tissue culture is a technique that cultivates isolated plant organs, tissues, cells and protoplasts on suitable culture media under sterile, artificially controlled conditions, enabling them to regenerate new cells, tissues or complete plantlets. Its theoretical foundation lies in plant cell totipotency—every single plant cell carries the capacity to multiply and develop into a full organism, just like Sun Wukong’s shape-shifting hairs.   This technology delivers an efficient, convenient and controllable approach for plant production and research. With continuous technical advancements, it has been widely applied in germplasm conservation, plant breeding, production of plant secondary metabolites, plant genetic engineering and other fields, yielding remarkable, fruitful outcomes.   A single parent plant can be propagated into thousands or even tens of thousands of tissue-cultured seedlings via this method. We can obtain large batches of clones that retain excellent agronomic traits while shortening production cycles, securing abundant material supplies for daily life. Today, it stands as one of the most dynamic and extensively applied modern biotechnologies.   2. What Is a Tissue Culture Laboratory?    A tissue culture laboratory is a dedicated facility for conducting plant tissue culture experiments. By regulating environmental conditions artificially to simulate natural plant growth, it enables rapid propagation, variety improvement, genetic transformation and other research objectives.   A standard tissue culture laboratory consists of six core functional zones: preparation room, washing & sterilization room, sterile operation room (inoculation room), culture room, buffer room and acclimatization room. Certain compartments may be combined or omitted based on actual site conditions. See the layout diagram below for reference.   Plant tissue culture requires strictly aseptic environments, so the lab must be equipped with laminar flow clean benches, analytical electronic balances, precision pipettes, autoclaves, stereomicroscopes, light incubators, biochemical incubators, air conditioners, refrigerators and other essential equipment.     II. How to Select a Suitable Clean Bench    1. Key Guidelines for Choosing a Clean Bench   A clean bench is a versatile purification device that delivers a localized high-cleanliness working zone. Selecting a qualified clean bench is the first step to guarantee sterile operations: it creates an aseptic workspace for operators, effectively prevents cross-contamination, and serves as a powerful tool to streamline experimental workflows.   Clean benches fall into two categories based on airflow pattern: horizontal laminar flow and vertical laminar flow. Horizontal laminar flow models feature fully open operation spaces, while vertical laminar flow benches are fitted with movable glass front sashes for flexible access. Users may select according to their experimental demands.   Premium materials and rational structural design form the foundation of sterile cultivation: •    The cabinet frame is constructed from high-quality steel with electrostatic powder coating; •    The working surface is made of full 304 stainless steel; •    The working chamber comes standard with LED lighting and UV germicidal disinfection systems, plus built-in waterproof backup power sockets; •    Optional side glass windows facilitate observation; single-person and double-person models are both available.   Its core function is generating a Class 100 ultra-clean workspace. An adjustable variable-speed fan system delivers uniform horizontal or vertical laminar airflow, paired with high-efficiency particulate air (HEPA) filters made of ultra-fine glass fiber media, achieving a filtration efficiency of ≥99.99% for particles sized 0.3 μm.   Stringent safety specifications are critical safeguards for sterile lab work: •    Built-in mechanical interlock system links lighting and UV disinfection functions; the UV lamp can only activate when the sliding sash is fully closed. If the front window is opened while UV is running, the ultraviolet lamp will shut off automatically. •    Optional delay timers and pre-set scheduling functions for disinfection cycles boost operational efficiency while protecting user safety.   An intuitive digital control interface upgrades user experience and optimizes sterile workflows. The standard embedded LCD controller displays real-time operational parameters including wind speed, light status, disinfection cycle and filter service life, with multi-mode audible

ACI Series CO₂ Incubators: Precise Control for Optimal Cell Culture Conditions I.    Product Overview A CO₂ incubator is laboratory equipment that simulates the in-vivo growth environment of cells and tissues inside its chamber to enable in-vitro cell and tissue culture. As an advanced instrument for cultivating cells, tissues and bacteria, it is indispensable core equipment for immunology, oncology, genetics and bioengineering research. It is widely adopted for research and production across microbiology, medicine, pharmaceuticals, environmental protection, food, animal husbandry and other scientific sectors.   A high-performance CO₂ incubator hinges on precise regulation of the cell culture environment, covering two core aspects: 1.    It delivers ultra-stable, highly accurate control over temperature, CO₂ concentration and humidity to facilitate smooth research workflows. 2.    It effectively prevents microbial contamination inside the chamber and enables regular decontamination, safeguarding research results and avoiding sample loss.     II.  Product Features   AIRTECH’s ACI Series CO₂ Incubators adopt direct heat jacket heating technology. Imported high-temperature-resistant IR sensors achieve precise regulation of temperature, humidity and CO₂ concentration. A high-efficiency microbial-grade gas filter is installed at the CO₂ inlet, boasting a filtration efficiency of 99.995% for particles ≥0.3 μm, which efficiently removes impurities and harmful aerosols from CO₂ gas. Paired with an intuitive full-color LED operation interface, the incubator delivers safe, simple and worry-free operation.   Precise Temperature Control—— Equipped with direct heat jacket heating and high-precision temperature sensors combined with closed-loop PLC millisecond-level computing, the temperature fluctuation inside the chamber is controlled within ±0.1°C.   Accurate CO₂ Concentration Regulation—— Imported high-temperature-resistant IR sensors work in sensitive linkage with vector regulating valves to stabilize CO₂ concentration within ±0.1%.   Rapid Parameter Recovery After Door Opening—— Proprietary active airflow control technology ensures fast recovery after door access: only 5 minutes for temperature restoration and 3 minutes for CO₂ concentration recovery even after a 30-second door opening.   Superior Thermal Insulation—— Specially engineered structures and high-enthalpy new materials minimize internal temperature and humidity loss and leakage. After a power outage lasting over one hour, the secondary temperature deviation inside the chamber remains below 2.5°C.   Active Condensation Control—— A dedicated condensation compartment collects condensate generated under high-humidity conditions in a designated area, eliminating secondary contamination caused by condensed water.   Complete Filtration System—— The CO₂ inlet is fitted with a high-efficiency microbial gas filter, achieving 99.995% filtration efficiency for particles ≥0.3 μm to intercept impurities and harmful aerosols in CO₂ gas.   User-Friendly Operation Interface—— A full-color LED controller paired with a high-performance microprocessor chip enables full-range monitoring and regulation of high-precision chamber parameters. Multi-level management controls guarantee intuitive, authentic display of operating parameters and performance metrics.   III.  About Us   AIRTECH integrates scientific research, product development, manufacturing and sales. It operates independent research institutes and laboratories, delivering comprehensive air purification technical solutions for diverse industries. Inheriting mature core technologies from Sujing Group while continuously introducing advanced air purification technologies from Japan and global markets, the company specializes in the R&D and production of cleanroom supporting purification equipment, including clean benches, biosafety cabinets, air showers, laminar flow hoods, sterile isolation systems, purification units, leak-resistant clean air supply ceilings and more.      

As years go by and time flows, every page of our journey bears witness to our diligent efforts day in and day out. On January 17, Sujing Airtech held its 2024 Year-End Summary & Commendation Conference alongside a Spring Festival Gala. Together, we look back on a year of hard work, honor the tireless dedication of every colleague, and envision the future as we stride hand in hand toward an even more brilliant era.   I. Annual Review & Work Plan   At the opening of the conference, General Manager Lu Dongfang acknowledged all remarkable achievements made by Sujing Airtech in 2024. On behalf of the company, she extended gratitude to every employee for their consistent hard work. Amid the severe headwinds of economic slowdown and cutthroat market competition in 2024, our team forged ahead to seize market opportunities. We weathered countless tests, growing stronger through experience, yet there remain areas ripe for improvement and refinement.   Following the recap, Ms. Lu laid out a comprehensive work roadmap for the new year. 2025 will bring fresh trials and challenges, and numerous tasks await our improvement and breakthroughs. Only by pooling our collective wisdom, standing united, staying grounded, taking solid action, and striving relentlessly can we overcome obstacles and deliver new outstanding results together. In closing, she wished everyone good health, all the best, a prosperous Year of the Snake, and happy families!     II. Commendation of Outstanding Staff   Next, Jin Zhen, Executive Vice Chairman of the company, took the stage to recognize employees with exceptional performance across all roles in 2024. Dedicated, passionate, and proactive at their posts, these role models have set benchmarks for all staff and fueled the steady growth of the enterprise.   Vice Chairman Jin remarked that despite fierce market competition in 2024, we never chose to stand idle—instead, we rose to challenges with proactive action. On behalf of the company, he expressed sincere thanks to all staff and their families whose relentless efforts drove positive progress for the business. On the journey ahead in the new year, every member of the team is the protagonist of our shared dream. Let us chase our aspirations hand in hand, for a better tomorrow is within reach.   II. Commendation of Outstanding Staff   That evening, all employees gathered for a celebratory feast. We raised our glasses in unison, cheering for a promising future for Sujing Airtech. The evening’s highlight was the Spring Festival lucky draw, where highly anticipated prizes were unveiled amid cheers and applause, lifting the festive atmosphere to new heights.    Dreams Are Distant, Yet Attainable with Perseverance; Aspirations Are Tough, Yet Realizable with Endurance! Let us regroup and march forward with unwavering resolve and boundless passion to embrace upcoming challenges. Through unremitting grit, fervent dedication, and a forward-thinking mindset, we will write an even more glorious new chapter for Sujing Airtech.