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The Sterility Test Isolator is a custom-designed cGMP Class A/ISO 5 isolator system, specifically engineered to provide the safest and most ergonomic working conditions for quality control operations.
Tailin hard-wall laminar flow sterility test isolator HTY series features a rigid structure made of stainless steel and tempered glass, creating a dynamic Class A internal environment.
Operations within the isolator are conducted using gloves, available in two versions: a thick, tear-resistant model and a thin, highly tactile option. The system incorporates a Siemens Programmable Logic Controller (PLC) for fully automated control of pressure and airflow volume and includes a pressure loss alarm function. Comply with GMP, USP, EP.
Sterile Assurance: HTY series isolators ensure the highest air quality within the isolation environment:
Automatic Leak Testing: Equipped with an automatic leak testing system that individually tests each chamber for leaks using the pressure decay method as described in international standard ISO 10648-2. Leakage rate is less than 0.5% /vol/hour under 2 times working pressure test.
Glove Integrity Testing: Equipped with an integrated automated glove leak testing system (GIT Series) which performs an independent leak test on each glove installed on the isolator system according to the positive pressure decay method described in the international standard ISO 14644-7. It detects holes as small as 100μm in diameter.
Data Management: Comply with 21 CFR Part 11 electronic records and signature requirements.
| Power Supply: AC380V/50Hz | Max.Power: 3000W-4000W |
| Cleanliness: GMP Class A | Chamber Pressure Range: From -80Pa to +80Pa |
| Airflow Direction: Laminar flow | Velocity: 0.36~0.54m/s |
| Built-in Sterility Test Pump: 1 or multiple | Compressed Air Supply: 0.4MPa-0.6MPa clean and dry |
| Killing Rate: ≥log6 | Noise: <75dB(A) when in pressure hold stage |
| Touch Screen: 12" Tablet PC | Leakage Rate: <0.5%/vol/hour under 2 times working pressure test |
| Vaporized Hydrogen Peroxide Residual Concentration: <1ppm | Cabin Illuminating: 500 lux, LED light source |
For GMP inspections of sterile pharmaceuticals, including sterile preparations and sterile active pharmaceutical ingredients.
For sterility tests, sampling, weighing, dispensing, etc.
Note: The sterility test, aseptic preparation and filling could be conducted in an isolator located whithin Class C/D, according to EU GMP Annex 1 and PIC/S<Recommendation on Sterility Testing> 8.1.1
Yes. The Tailin HTY Series Sterility Test Isolator can be fully customized in size and configuration to meet specific GMP laboratory layouts and process requirements for sterility testing and quality control.
A wide range of optional accessories can be configured to enhance system capability, traceability, and operational efficiency, including:
Tailin provides comprehensive validation support and documentation packages, including:
Absolutely. The HTY Series Isolator complies with GMP, USP, EP, and 21 CFR Part 11.