In aseptic manufacturing, glove testing has always been a weak link in maintaining microbial integrity for barrier systems such as isolators and RABS. Any undetected micro-defects may evolve into a fatal path leading to product contamination.
For this reason, EU GMP Annex 1 “Manufacture of Sterile Medicinal Products” places unprecedented emphasis on glove integrity. The regulation requires that enterprises’ Contamination Control Strategy (CCS) must fully consider the potential impact of barrier or glove integrity breaches during risk assessment. Meanwhile, it also provides clear guidelines on testing methods and frequency.
According to EU GMP Annex 1, 22.8.2022 C(2022) 5938 final:
4.21 The materials used for glove systems (for both isolators and RABS), should be demonstrated to have appropriate mechanical and chemical resistance. The frequency of glove replacement should be defined within the CCS.
Reference: https://health.ec.europa.eu/system/files/2022-08/20220825_gmp-an1_en_0.pdf
It is evident that traditional experience-based testing methods can no longer meet compliance requirements. A systematic, high-frequency, and data-traceable testing model will become the mainstream practice in the industry. The Parenteral Drug Association (PDA) points out that modern glove testing systems should be designed to meet the requirements of “Pharma 4.0” for control connectivity, reporting, and data integrity management.
To better address regulatory requirements and industry trends, Tailin has launched the next generation of its Wireless Glove Integrity Tester – the GIT-WLAN03.

Guided by the “Quality by Design (QbD)” concept, this product achieves wireless device communication, paperless data, and in-situ testing through wireless communication and intelligent software technology. The testing system supports multi-device group control and data interconnection, automatically generates electronic test reports that comply with GMP requirements, and builds a closed-loop data ecosystem covering the entire process.
The testing system strictly adheres to the industry-recognized ALCOA+ principle, ensuring all data meets the following characteristics:
Benefiting from the integration of wireless communication and self-developed SCADA (Supervisory Control and Data Acquisition) Management Software functions, the compliance of test data can be guaranteed even when the device is in remote communication status:
The system has a built-in tamper-proof audit log function. Every operation—from user login, parameter setting to test report generation—is fully recorded. The log file includes key fields such as timestamp, operating user, specific operation, and electronic signature notes, ensuring all activities are traceable.
In group testing mode, each tester is equipped with an independent user login function. Therefore, even when operating multiple devices simultaneously, the central management software can accurately track the operator information for each device, implementing “attributability” of data in every detail.
The system uses a professional SQL Server Database to archive and store all process data. Users can not only customize backup plans to ensure long-term storage but also leverage powerful multi-dimensional query functions to quickly retrieve historical data and logs by criteria such as time, device, operator, and test results—making data accessible whenever needed.
Complete and reliable test data can provide important basis for quality decisions, supporting the maintenance and improvement of management systems:
Against the backdrop of increasingly stringent industry regulations and compliance requirements, glove integrity testers are not only testing tools but also key guarantees for enterprises’ compliance management. With electronic signature and audit trail functions, the product provides the industry with an efficient, intelligent, and compliant solution, supporting enterprises in safe, efficient, and compliant production and operation.
Contact us: marketing@tailingood.com