The Aseptic Filling Isolator features a three-chamber design, comprising a transfer chamber, filling chamber, and capping chamber. An integrated Vaporized Hydrogen Peroxide (VH₂O₂) sterilization system enables the chambers to be sterilized either individually or simultaneously. With modular assembly and automated production, the system improves aseptic preparation efficiency while minimizing the risk of contamination during the filling of aseptic preparations and ATMPs. Custom configurations are available to meet specific customer requirements.
The Tailin Containment Isolator is a negative-pressure solution specifically designed for ADC small-molecule synthesis and the handling of highly potent pharmaceutical compounds. Meeting OEB5 personnel-protection requirements with an OEL below 0.05 µg/m³, the system combines H14 HEPA filtration, internal explosion-proof protection, and continuous-liner material transfer to safeguard operators, products, and the surrounding environment. Multiple processes—including rotary evaporation, filtration, drying, weighing, dispensing, and capping—can be integrated into one secure and efficient closed system.
The Tailin Containment Isolator is specifically designed for crude peptide dissolution during active pharmaceutical ingredient processing. Meeting OEB5 design requirements with an OEL below 0.1 µg/m³, the system incorporates a liquid-dispensing container to support continuous weighing and feeding operations. Its fully explosion-proof design meets EX d II BT4 requirements, helping protect operators, control material dispersion, and improve process safety when handling highly potent peptide materials.
The Tailin Containment Isolator is a negative-pressure system designed to protect operators during the weighing, dispensing, and sampling of highly potent powders and products. Meeting OEB5 personnel-protection requirements with an OEL below 0.05 µg/m³, the system supports weighing accuracy of up to 1/1,000,000 and incorporates both a continuous liner system and Rapid Transfer Port. Its enclosed and controlled working environment helps minimize occupational exposure, prevent cross-contamination, and improve safety in pharmaceutical laboratories and manufacturing facilities.
Filling & Packaging Machine
DCSmart is an intelligent capping machine designed for pharmaceutical vials fitted with aluminum or aluminum-plastic caps ranging from 8 to 33 mm. Combining full servo drive, digitally adjustable segmented torque, and wireless HMI connectivity, the system delivers a capacity of 420–600 vials per hour. Recipe versioning, audit trails, batch records, electronic signatures, and PDF report export enhance data traceability across pharmaceutical, biotechnology, and R&D applications.
The isolator is designed to provide maximum protection for both operators and products, fully meeting OEB5 containment requirements with OEL < 0.05 μg/m³. It integrates H14 HEPA filtration, a continuous liner system, RTP, and Siemens PLC control, ensuring safe operation under a general background while maintaining a static Class C internal environment. The system is ideal for high-potency material handling, precision weighing, and critical pharmaceutical and laboratory applications.
Isolator
Tailin MLFC is a ready-to-use solution designed for the precise filling, stoppering, and capping of vials, providing a practical platform for clinical trials, process development, and small-scale pharmaceutical production. With a focus on high-precision quantitative filling, the system is well suited for demanding applications in pharmaceutical and biotechnology development, including products such as lentiviral vectors and gene therapies. Supporting vial sizes from 2 mL to 100 mL, Tailin MLFC offers the flexibility needed across different development stages. The system can be integrated into laminar flow cleanrooms, isolators, or RABS, helping maintain controlled aseptic conditions throughout the filling process.
Reliable Sterility Protection with Continuous Grade A Environment The Tailin CST Series Sterility Test Isolator is designed for critical aseptic processes such as sterility testing, dispensing, and sample handling. By combining a physical barrier with efficient VH₂O₂ biodecontamination, the system maintains a continuous GMP Grade A environment, minimizing the risk of external and cross-contamination. - Continuous GMP Grade A environment - Efficient VH₂O₂ biodecontamination - Reduced contamination risk - Continuous or batch operation - Designed to meet EU GMP, FDA cGMP, and USP-NF requirements
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