Empowering Glove Integrity Testing: Successful End User Training on the Esco IntelliGlove Tester (EIGT) in Bangladesh
Esco Lifesciences Bangladesh Pvt Ltd recently conducted an End User Training session on the Esco IntelliGlove Tester (EIGT) at one of the leading pharmaceutical companies in Bangladesh. The training was designed to equip the client’s technical team with the practical skills and insights needed to perform reliable glove leak testing, ensure compliance with industry standards, and uphold the rigorous safety and quality requirements of controlled environments in pharmaceutical manufacturing.
The training was met with engagement and enthusiasm from participants, who actively participated in discussions and hands-on demonstrations. From detailed product operation to best practices in routine testing, the training reinforced our commitment to empowering users with confidence and competence in deploying advanced contamination control tools.
Building Local Expertise Through Training
Esco’s end user training in Bangladesh went beyond product introduction. It focused on equipping attendees with the hands-on skills, operational knowledge, and best practices needed for effective glove leak testing. Participants learned how to:
- Set up and operate the EIGT in real-world workflows
- Interpret test results with confidence
- Utilize traceability and documentation functions for compliance
- Incorporate glove integrity testing into routine quality programs
The client’s team demonstrated strong engagement and technical curiosity, reinforcing the value of structured training in maximizing the benefits of advanced technology adoption.
The Esco IntelliGlove Tester (EIGT)
The Esco IntelliGlove Tester (EIGT) represents Esco’s third-generation wireless glove leak tester, engineered for precision and usability in today’s advanced aseptic and containment environments. Built around the pressure loss testing principle defined in ISO 14644-7, the EIGT reliably detects leaks and integrity breaches in gloves, sleeves, and gauntlets used in isolators, Restricted Access Barrier Systems (RABS), and glove boxes — all critical components of sterile manufacturing workflows. Routine verification of glove integrity, as supported by this system, is essential for ensuring contamination-free operations in pharmaceutical and biocontainment facilities. These features make the EIGT not just a testing tool, but a comprehensive solution that supports robust contamination control strategies, minimizes human error, and strengthens sterility assurance programs.
Key Features of the EIGT
The EIGT is equipped with a range of advanced features that enhance both its performance and ease of use:
- Wireless, Portable Design –
Facilitates flexible testing around isolators and barrier systems without
the clutter of cables or hoses.
- ISO 14644-7 Pressure Change Testing
– Supports consistent and standardized leak detection in line with global
cleanroom standards.
- Compliance with EU GMP Annex 1 Expectations – Helps users align with contamination control expectations
outlined in updated regulatory guidelines.
- Integrated Touch Display –
Simplifies operation with intuitive controls for inflation and deflation
cycles.
- Supports 21 CFR Part 11 – Software
features audit trails, secure electronic records, and documentation for
compliance and traceability.
- Connectivity Options – Built-in
Wi-Fi and Modbus TCP/IP support seamless integration with facility
automation and data management systems.
- Traceable Testing & Full Documentation – Enables reliable record-keeping with secure audit logs and test histories.
Target Markets and Applications
The EIGT is ideal for a wide range of pharmaceutical
and biocontainment markets, addressing the needs of highly regulated
environments where glove integrity is critical:
- Aseptic Manufacturing Facilities –
Supporting routine integrity checks in isolators and RABS.
- Quality Control Laboratories –
Enabling documented verification as part of release and compliance
testing.
- Biopharmaceutical Production –
Ensuring contamination-free environments in sterile drug and biologics
manufacturing.
- Cleanroom Operations – Complements
broader contamination control strategies required for ISO classified
cleanrooms.
- Regulated Environments (FDA, EMA, WHO) – Helps users meet regulatory expectations for controlled zone
integrity verification.
By catering to diverse global markets —
from pharmaceutical manufacturing and biotech processing to regulatory quality
labs — the EIGT contributes to safer, more efficient, and compliant operations
worldwide.
We extend our appreciation to the client
for their active participation and dedication throughout the training. This
collaboration underscores our shared commitment to quality assurance,
regulatory compliance, and operational excellence in pharmaceutical
manufacturing.
For more information about the Esco
IntelliGlove Tester (EIGT), visit the product page and watch the product video:
🔗
Product information:
https://www.escopharma.com/products/intelliglove-tester-eigt-wireless-glove-leak-tester/61
🎥 Video overview: https://youtu.be/A4udaP3C1Yc?si=LV_Hhb7OGAumAZuu
