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Automatic Detection System forCryptosporidium and Giardia
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Container Closure Integrity Tester (CCIT)
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Improve the accuracy of coliform testing using enzyme substrate methods. Tailin explores solutions for common challenges, including residual chlorine neutralization, heavy metal interference, and optimized incubation strategies to ensure compliance with ISO and U.S. EPA standards.
Understand how Biological Indicators (BIs) and Chemical Indicators (CIs) work together in VH2O2 Sterilization decontamination. Learn about EU GMP Annex 1 compliance and 10⁻⁶ SAL validation for aseptic isolators.
Explore how Tailin HK200 Hydrogen Peroxide Gas Concentration Analyzer optimizes VH2O2 sterilization in food & beverage aseptic filling. Achieve 31.5% higher concentration, 50% better stability, and prevent condensation via real-time dew point monitoring.
Tailin introduces the new Immutailin™ PVDF blotting membrane with high protein-binding capacity, excellent chemical resistance, and superior sensitivity for Western blot and protein detection. Free sample available until June 30, 2026.
In the pharmaceutical landscape, the rise of oncology drugs, ADCs (Antibody-Drug Conjugates), and innovative hormonal therapies has brought High Potency Active Pharmaceutical Ingredients (HPAPIs) to the forefront.
Tailin MD500 Microbial Detection Analyzer Passes Authoritative Validation, Accelerating Compliance in Pharmaceutical Testing.
Filtailin® XA Series PES membrane from Tailin is engineered for biopharma filtration, combining an hourglass asymmetric structure with high throughput, low protein adsorption, and reliable performance under repeated 121 °C steam sterilization.
Mixed Cellulose Ester (MCE) microporous membranes represent the earliest commercially produced variety of microporous membranes, with a history spanning over a century.
Scaling Strategic Innovation: Tailin Breaks Ground on Advanced Materials & High-Performance Membrane Facility. This strategic facility integrates R&D, production, and validation to enhance industrial autonomy.
In the pharmaceutical industry, vial sealing integrity is the ultimate safeguard for drug safety—meeting global regulatory standards. Traditional capping solutions often lack consistency and traceability, which can lead to compliance risks.
From FDA warning letters to 2025 Chinese Pharmacopoeia rules, "complete" microbial data is non-negotiable—traditional manual processes fall short. Tailin's automated solutions (SCW/ASC/AST Series) bring full traceability, real-time monitoring, and 21 CFR Part 11 compliance to close data gaps.
Tailin Honored as "Advanced Committee Unit for Standardization Work" for Supporting Domestic & International Sterilization Standardization
