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TOTAL SOLUTION

Q: Measuring range (specimen size)

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CONFIGURE EXPERIENCE

MEASURING RANGE

Various

FORCE RANGE

0-20 N

PARAMETERS

3

APPLICATION

Softgel Capsule

THE NEW GENERATION OF GELOMAT IS A TECHNOLOGY BREAKTHROUGH IN SOFTGEL CAPSULE HARDNESS TESTING, ENGINEERED TO CARRY FORWARD THE UNDISPUTED STANDARD OF THE INDUSTRY’S RENOWNED GELOMAT.

A Legend, Reimagined

The Gelomat 2 is a complete makeover of the original Gelomat in every aspect. It is a solution that delivers measurement precision on par with the iconic Gelomat while increasing its testing throughput with a built-in automated capsule conveying & positioning system. In terms of 21 CFR Part 11 compliance, the Gelomat 2 provides instrument-level control of user permissions and traceable activity logs. This next generation of the Gelomat is by all means the world’s most advanced softgel capsule testing system.

ALL SIZES,
ALL SHAPES

The Gelomat 2 conveying system automatically positions each capsule for accurate and repeatable testing. The fixture accommodates virtually every capsule size and shape reducing setup hassles and operating costs.

STANDALONE 21 CFR PART 11 COMPLIANCE

Powered by the latest embedded technology, the Gelomat 2 features integrated user management and audit trail functionality directly on the instrument, eliminating the need for additional software.

SLEEK AS IT LOOKS, SMART AS IT FUNCTIONS

The Gelomat 2 shares the same design DNA as the THT500 – the Red Dot Award-winning product. At Bareiss Pharma, we believe that even a machine can have style that makes it pleasant to work with.

GELOMAT 2 STAYS MODULAR

The core of the Gelomat 2 is a plug-and-play high- precision measuring device that can be easily dismantled for service or calibration.

MAX YOUR TEST THROUGHPUT

Load up to 10 samples at a time. The Gelomat 2 automatically conveys, positions, and tests each sample before printing or saving the results directly on the instrument. Data can also be exported to Celeste software for further analysis.

IT IS ALL ABOUT COMPLIANCY

Gelomat’s 21 CFR Part 11 compliance ensures secure, trustworthy data. Features like audit trails and electronic signatures help pharmaceutical manufacturers maintain data integrity, streamline GMP workflows, and easily meet FDA requirements.

“BAREISS IS BACKED BY THE WORLD’S MOST RENOWNED

PHARMACEUTICAL COMPANIES“

EXPERIENCE YOURSELF

Request a Bareiss demo unit delivered to your door. There is no better way to choose your perfect testing instrument than by experiencing it before buying.

LEARN MORE

GVT 20 FAQS

Here we answer the most common questions about the Bareiss Gelomat 2. If you can’t find the answer to your question, please see the full list by clicking the link below.

TOTAL SOLUTION