Ensure reliable integrity testing for your transfer systems
Detect and prevent leaks in alpha ports, beta containers & other RTP systems.
You test your gloves – but not your alpha ports or beta containers? Leaks don’t just compromise product sterility; they put your employees and patients at risk. The RTP Tester from MK Versuchsanlagen closes this gap, ensuring safety and compliance before contamination can occur.
Safety first!
While glove integrity testing is already a mandatory requirement under Annex 1, there is currently no such a strict regulatory obligation to test transfer ports or containers than for glove testing – however, due to current regulatory discussions, its expected that this will become increasingly strict and the industry is already preparing for this.
At the same time, the contamination risk associated with these interfaces is equally significant. Every transfer step represents a potential breach point — and regulators are increasingly emphasizing holistic contamination control across all barrier components. The RTP Tester enables you to address this risk proactively. With highly sensitive pressure decay testing, even the smallest leaks in alpha ports, beta containers, and other transfer systems seals are detected within minutes helping mitigate a contamination incident before it happens. This allows you to strengthen your contamination control strategy today and prepare for future regulatory expectations.
Discover how the RTP Tester can safeguard your transfer systems, before regulations make it mandatory:
Why choose MK RTP Tester?
Maximum Safety
Pressure decay test detects even the smallest leaks before they become a hazard
Adaptable Design
Configurable sealing unit fits your specific transfer system setup
Smart RTP Container Management
And comprehensive service options
Compliance assured
Supports FDA, cGMP, and EU GMP Annex 1 requirements
German Quality
Designed and manufactured to the highest safety and quality standards
Flexible Integration
Compatible with Alpha Ports, Beta Containers, and other transfer systems
Fast Testing
Individually configured parameters enable quick and efficient leak detection
Enterprise Ready
MES integration, Wi-Fi (WPA2 encrypted), and RFID for software-based testing
Automated Documentation
PDF test reports, user management, and complete data integrity
By integrating the RTP Tester:
You enhance process safety, protect both product and personel and ensure that critical transfer steps remain controlled and verifiable – even in the absence of formal regulatory requirements.
Your Benefits
Minimized Downtime
Maximum Process Reliability
Future-Proof Compliance
Transparent Documentation
More about RTP Tester
More Information about MK RTP Tester
Frequently Asked Questions
We answer the most common questions about MK Pilot Plants
What does MK Versuchsanlagen do?
MK Versuchsanlagen GmbH & Co. KG, based in Mücke-Merlau (Hesse, Germany), has specialized since 1988 in metal-free laboratory systems, cleanroom technology, and automated Glove Testing Systems.
The company develops and manufactures customized solutions for the pharmaceutical, life sciences, semiconductor, and optics industries – from contamination-free cleanrooms made from metal-free materials to Glove Integrity Test Systems (GITS®), as well as custom software and Industry 4.0 electronics. Production is carried out entirely in-house, certified according to ISO 9001:2015 and at the highest quality level.
Who is behind MK Versuchsanlagen?
MK Versuchsanlagen is a family-owned company based in Mücke-Merlau (Hesse, Germany), founded in 1988 by Michael Keil. As managing director, he continues to shape the strategic direction and technological innovation of the company.
The management team combines deep technical expertise, years of industry experience, and a strong vision for quality, innovation, and customer proximity.
The company culture emphasizes personal responsibility, close cooperation with customers worldwide, and a strong focus on sustainable manufacturing “Made in Germany.”
All development, design, software and hardware engineering, and manufacturing are carried out by a dedicated team at the company’s headquarters in Central Hesse.
What are the benefits of an automated Glove Testing System?
An automated Glove Testing System like our MK Glove Integrity Test System (GITS®) offers a fast, safe, and fully documented method for testing the integrity of gloves used in isolators or RABS (Restricted Access Barrier Systems) – without interrupting production (in-situ).
Your benefits at a glance:
- Time-saving: Simultaneous testing of all gloves – test times from 5 minutes (depending on material and glove size)
- GMP & Annex 1 compliant: Meets EU GMP Annex 1, FDA 21 CFR Part 11, and GAMP 5 requirements
- Traceability: Automated documentation, data transfer, and reports – integrable into your Contamination Control Strategy (CCS)
- Wireless operation: No disruptive cables, easy cleaning, compatible with H₂O₂ / VHP decontamination
- Smart features: RFID-based port and glove recognition and GLCS® for glove lifecycle monitoring and defect detection
- Flexible integration: Operates as a standalone system or can be fully integrated into existing setups
GITS® is a reliable Glove Testing System that improves efficiency while ensuring maximum safety.
Why are Glove Testing Devices needed?
Glove Testing Devices ensure the tightness and integrity of gloves used in isolators and RABS systems. These gloves form a critical barrier between product and operator – even minor leaks can lead to contamination or batch failure.
An automated Testing System enables:
- Reliable integrity testing before, during, or after production
- Compliance with regulatory requirements (e.g., EU GMP Annex 1)
- Complete documentation and traceability
- Safe pharmaceutical manufacturing without compromising product or personnel safety
In short: Glove Testers secure your processes, protect your products, and help maintain the highest quality standards.
How are gloves tested for leaks?
Glove integrity is typically tested in cleanroom or isolator environments using automated pressure decay tests.
The glove is inflated with air for a defined period, and the system monitors how fast the pressure drops – which can indicate leaks such as microcracks or pinholes.
Modern systems like the MK Glove Integrity Test System (GITS®) perform these tests automatically, wirelessly, and software-assisted, including:
- RFID-based identification of glove and port
- Simultaneous testing of multiple gloves (e.g., on an isolator)
- Automated documentation and evaluation of all results
- Full compliance with GMP and Annex 1
This ensures that only compliant gloves are used in production – for maximum product safety and process reliability.
What is the Transfer System Tester (TST) used for, and what are its benefits in pharmaceutical environments?
The Transfer System Tester (TST) is a specialized device for integrity testing of Rapid Transfer Ports (RTP), alpha ports, and beta containers.
It enables fast, automated testing via pressure decay and reliably detects even the smallest leaks.
As an RTP tester, the TST can be flexibly adapted to various RTP containers and port systems.
Thanks to integration options with existing systems such as GITS®4 or GLCS®, and features like WLAN and RFID recognition, the TST offers maximum process security, full traceability, and supports compliance with regulatory standards such as EU GMP Annex 1, 21 CFR Part 11, and GAMP 5 – all with minimal impact on production workflows.
What is the Glove Life Cycle System (GLCS®), and how does it support cleanroom process safety?
The Glove Life Cycle System (GLCS®) enables complete traceability of glove usage within cleanrooms.
Using RFID technology, the software automatically documents storage, sterilization, aging, and cleaning of each glove.
If predefined limits are exceeded, the system issues warnings or blocks testing automatically.
This ensures that unsafe gloves are reliably identified, enabling compliant and safe glove use in accordance with GMP standards – while also highlighting early wear and reducing unnecessary glove consumption, thus supporting both process safety and environmental sustainability.
What are the benefits of the Analysis & Reporting Tool (ART) for evaluating GITS® and GLCS® data?
The Analysis & Reporting Tool (ART) is a centralized platform for generating and evaluating reports from GITS® and GLCS®.
It produces machine- and port-specific reports, audit trails, and freely configurable evaluations.
With centralized data collection, trends can be identified, weaknesses analyzed, and informed decisions made.
ART is 21 CFR Part 11-compliant, fully network-capable, and supports both electronic and automated printouts – ideal for audits and quality assurance documentation.
Contact
Contact us for guidance on your project
Talk to our experts.







