Cap Torque Tester HP-100  It is used for testing the lock and open torque of the bottle cap for pharmaceutical packaging. Combined with leakage tester it can measure the sealing of medicine bottles.

GC9802-K Face Mask Ethylene Oxide (EO) Residuals Testing Gas Chromatography has a reasonable structure, stable and reliable performance, simple operation and convenient maintenance. Can be widely used in petroleum, chemical industry, pesticides, medicine and health, commodity inspection, environmental protection, universities and other production and scientific research departments. It can be used to detect ethylene oxide and other organic solvents. Detects purity or content of a single solvent

Application Use for test the light transmittance and haze degree of all transparent and semi-transparent parallel plane samples (plastic plate, sheets etc), and turbidity or clarity of liquid samples (water, drinks etc), used in the industries of plastics, membrane, coatings and paints, printing ink, research institute and so on.

Medical Mask Exhalation Valve Air Tightness Tester  is Used to detect the air tightness of the mask breath valve. GBPI offers mask testing machines for surgical face masks, N95 masks, Melt-blown fabric. BFE Tester, PFE Tester, N95 Tester, Melt-blown fabric Tester      

full-automatic migration tester is specialized for testing dissolved non-volatile-matter of materials after soaked in specific solution.

The torque tester is professionally suitable for testing the torque value of the caps of packaging products such as bottles, beverage bottles, mineral water bottles, and milk bottles. It is an ideal configuration instrument for offline or online testing of production units in the packaging industry.

AUTO GBM‑L2 Dual‑Pressure Micro‑Leak Seal Tester: Micro‑Leakage Detection for Pharmaceutical & Food Packaging GBPI AUTO GBM‑L2 Dual‑Pressure Micro‑Leak Seal Tester for Packaging Micro‑Leak Detection Product Introduction AUTO GBM‑L2 Dual‑Pressure Methods Vacuum Decay Leak Detection Tester adopts the test principle of vacuum decay method/pressure decay to detect micro‑leakage of finished packaging. It can be applied to packaging systems composed of vials, ampoules, pre‑filled syringes, eye drop bottles, HDPE bottles, infusion bottles/bags and other pharmaceutical packaging, food packaging, and chemical industry packaging. Testing Principle The host is connected to a sealed test chamber customized according to the sample. When performing the vacuum decay method test, the instrument evacuates the test chamber, and a pressure difference is formed inside and outside the sample. Under the action of the pressure, the gas/liquid in the sample enters the test chamber through the leak hole. The main engine uses the absolute pressure sensor and the differential pressure sensor to monitor the pressure change in the chamber to judge whether the sample leaks. When performing the pressure decay method test, the instrument fills the test chamber with a predetermined air pressure, and the gas in the test chamber enters the sample through the leak hole. The host uses absolute pressure sensors and differential pressure sensors to monitor the pressure changes in the chamber to determine whether the sample is leaking. Executive Standards ASTM F2338‑2009(2013), YY‑T 0681.18‑2020, USP<1207.2>, ASTM F2095, supporting leakage verification for global pharmaceutical and food packaging regulatory requirements. Core Technical Parameters Absolute Pressure Testing Range (0‑300) kPa Differential Pressure Testing Range (-2‑2) kPa Detection Sensitivity 1‑3 μm Balancing / Testing Time 1‑3600 s Vacuum Purge Time 1‑3600 s Set Flow Rate 0‑3 mL/min Testing System Dual Sensor Technology / Dual Cycle Testing Testing Chamber Customized according to the sample Applicable Products Vials, Ampoules, Prefilled Syringes, Infusion Bottles/Bags, etc. Detection Principle Vacuum Decay Method / Pressure Decay Method Dimensions of the Main Unit 495 mm*455 mm*280 mm Ambient Temperature 20℃‑25℃ Relative Humidity 40%‑60% Working Power Supply AC 220V, 50HZ Product Features • Dual‑Pressure Methods, to help solve testing difficulties. The double combination of vacuum decay method and pressure decay method solves the problem of easy misjudgment and false negative for freeze‑dried powder injections containing vacuum in the bottle using a single vacuum decay method. Based on dual‑sensor and dual‑circulation system technology, high‑quality absolute pressure sensor and differential pressure sensor, with an accuracy of 0.1% FS, can effectively detect large and small leaks, accurately calculate the leak hole diameter, and give a pass or fail judgment. • Low detection sensitivity and good test repeatability. For rigid samples, the detection sensitivity is as low as 1 μm, and the test repeatability is as low as 0.8%. The instrument has stable performance, low noise and good repeatability. • Imported brand accessories, excellent performance. Imported brand vacuum pump, pumping rate up to 3 L/s, noise as low as 50 DB, high ultimate vacuum, convenient oil level detection and replacement. The imported gas mass flow controller can simulate micro‑leaks arbitrarily, with a resolution of 0.001 mL/min, which provides a reliable guarantee for the method verification of instrument sensitivity. • Large‑size touch screen, intelligent operation. Color 7‑inch touch screen, clear view, sensitive touch, easy to operate. Equipped with a micro‑printer, USB data interface, and supports PC software measurement and control operation. The test software is designed according to the GMP appendix "Computerized System". It has an audit trail function and multi‑level authority settings for users, which can meet the needs of the pharmaceutical industry for data traceability. • Personalized customization to meet the needs of different samples. For different test samples, it supports customization of suitable test chambers to meet the needs of different tests. For the same type of samples, it supports customized nesting mode, which can realize the sharing of a test chamber for samples of various specifications. Application Fields Freeze‑dried powder injection Injection Prefill needle Eye drops Plastic Ampoule BFS Infusion bags Factory Configuration Standard Host machine, vacuum pump, test chamber and 3 sets of yin and yang control (customized as required), 11‑inch touch panel, professional software (GMP) Optional Imported gas flow meters, air compressors, printers, calibration certificates Conclusion AUTO GBM‑L2 dual‑pressure micro‑leak seal tester combines vacuum‑decay and pressure‑decay technology, solving false‑negative defects existing in single‑mode leak detection for vacuum‑containing pharmaceutical containers. With imported core components, audit‑trail data function and customizable test chamber, it is ideal micro‑leakage inspection equipment for pharmaceutical factories, third‑party testing laboratories and R&D institutions for parenteral preparation packaging quality control. Get Quotation for This Unit GBPI Packaging Test Equipment ManufacturerAddress: No.3 Linjiang Road, Xiagang Subdistrict, Huangpu District, Guangzhou, Guangdong, ChinaTel: +86 15820231129 | Official Website: www.gbpitester.com

Water Vapor Permeability Analyzer -AUTO W809 is designed and manufactured in accordance with ASTM E96, GB/T 1037 standards, and provides a wide range of high-efficiency water vapor transmission rate testing for low, medium and high water vapor barrier materials with the  principle of Gravimetric Method.

    LIMS Intelligent Laboratory Management System One-stop All-round Lab Information Management About GBPI & LIMS Overview Founded 2002, GBPI supplies packaging test instruments & lab solutions, with CNAS testing center serving global food/pharma/material labs. Self-developed LIMS eliminates manual lab defects, auto-collects data, full traceability for Man/Machine/Material/Method/Environment, user-friendly all-in-one lab management. LIMS System Homepage All-in-One Lab Digital Ecosystem LIMS/SDMS/LES/ELN PLM/CRM/Warehouse IoT & Data Analysis Dashboard & Mobile App Modular unified data platform, auto workflow, full traceability, cuts manual bottlenecks & meets multi-site compliance demands. Core Lab Capabilities ●Resource scheduling & test plan management ●Sample & document centralized archive ●Auto generate compliant custom reports ●Auto data acquisition & trend analysis ●Barcode sample full lifecycle traceability Platform Supported Operations ●Abnormal data alert & intelligent review ●Auto result vs specification comparison ●Auditable electronic record management ●Personnel/equipment/sample integrated control ●Data analytics & full compliance audit trail Platform Core Strengths All core lab modules integrated, no third-party docking cost, fast deployment, data analytics & full lifecycle QC for standardized lab management. Rapid Industry Deployment Pre-built industry templates, fully customizable lab workflows. Intelligent Data Analysis Visual dashboard delivers real-time data for precise decisions. Full Lifecycle Management Full QC covering sample entry to final report output. Compliance & Traceability Built-in audit trail & e-signature to meet regulatory standards. Core Competitive Advantages Web access,no install,multi-industry fit Auto bilingual reports,QR paperless share PC&mobile remote equipment schedule Barcode sample register & storage visualization IoT remote virtual lab monitoring Smart resource allocation & third-party test support Standard Business Workflow Sample Login ➡️ Sampling & Receipt ➡️ Resource Planning ➡️ Data Analysis ➡️ Review & Approval ➡️ Report Output Multi-Module Collaborative System Business & Contract Management Order tracking,digital contract & intelligent quotation Sample & Equipment Management Full sample traceability,remote equipment monitoring Testing & Report Management Auto test records,custom reports & real-time data share Quality & Security Management QC control,role permission & full audit management   Full-Lifecycle Professional Service One-stop customized LIMS service including consultation,development,deployment & after-sales support,tailored for all lab scales & industries. 1 Planning Kickoff & training 2 Development Custom configuration 3 Testing Function verification 4 Preparation Audit & user training 5 Deployment Online launch & acceptance Pharma & Biotech Custom Solution Compliant LIMS for pharma/biotech labs, meets FDA audit standards, full data traceability & multi-site collaborative quality control. Integrated Platform Management Unified R&D/test/production data archiving & monitoring. Professional Lab Workflow Full control of instrument,inventory,testing & reporting. Strict Compliance Guarantee Built-in audit workflow to pass pharmaceutical regulatory inspection.

The popular single-guidance electronic tensile testing machine GBL-H is a mechanical property testing machine developed and manufactured by the Guangzhou Biaoji R&D team based on GB, JIS, ASTM and other standard requirements and market demands. The instrument adopts high-precision sensors, and the force measurement accuracy is within ±1 %FS; professional software support, fully automatic operation, equipped with liquid crystal display screen, real-time display of test curve data and query test report, convenient and fast testing; Choose built-in or external, with perfect limit protection, overload protection, emergency stop and other safety protection functions.

A533 water vapor permeability analyzer is to test the water vapor transmission rate (WVTR) of films or sheets materials.

Application GNP-1 Bursting Strength Tester can measure the bursting strength of single-layer or multi-layer paper, and can be used to test the blasting strength of cloth, leather, paper board, thin metal sheet, etc. Use mark transmission pressure, automatically retain the maximum bursting strength value when bursting, decomposition degree is 100 times higher than the needle type.