The Kaye product range is relied upon by the world’s leading pharmaceutical and biotechnology companies to validate and monitor critical assets and processes like sterilization as required by governing regulatory bodies.
Kaye LabWatch IoT powered by FCX is an intelligent Cloud based monitoring system designed for Life Sciences, to continuously monitor, alarm and collect critical GxP data for analysis, reporting and real-time actionable knowledge.
Find your direct and local support. Reach out to our Kaye team or our authorized partner in your region for your sales enquiries, technical or services support. We look forward to assisting you with all your thermal validation system, environmental monitoring, and cold chain needs.
The Common Reporting Tool software is a comprehensive reporting utility that can be installed on a separate Windows PC and allows you to generate reports from AVS or ValProbe RT Qualification study files in order to document the results of your validation studies.
Elevate your work and stay connected with the unique Kaye Keyboard, designed to seamlessly integrate with the Kaye Tablet Console. Experience convenient features that transform the way you work on the go.
In today's rapidly evolving digital landscape where Pharmaceutical and Biotechnology companies depend on accurate and reliable data, it is essential that reporting is streamlined and flexible. With the introduction of their latest software version 2.0 for Validator AVS, Kaye proudly presents a significantly enhanced reporting tool with simplified User Management capabilities.
Introducing the Kaye IRTD Display, a standalone interface with a touchscreen. This advanced display unit seamlessly connects with up to two Kaye IRTD Reference probes, offering real-time temperature data in a user-friendly format. Equipped with a 4.3" touch screen, the Kaye IRTD Display provides clear and intuitive readings for both IRTDs, allowing users to monitor temperature with ease.
The HygroCal100 provides a stable test chamber to quickly evaluate the performance of Kaye’s ValProbe RT Humidity Loggers or any relative humidity sensors across a wide range of 5 to 95% relative humidity. The intuitive design allows up to 8 probes or loggers under test to be easily sealed and immersed in the chamber. Typically the HygroCal100 is controlled by the ValProbe RT Software for automated Verification runs but alternatively the unit can also be controlled by the 4.3” LCD touch-screen, that runs a powerful UI, which displays all measured values from the reference along with a graphical trend indication of chamber stability. If not used with the Kaye ValProbe RT Loggers the HygroCal100l is also capable of automating complete validation procedures with ease, and providing a complete logged output in csv format straight to your USB memory device, to minimize the time you spend taking readings.
Mar 21, 2024
Cryo containers are found in various applications in the pharmaceutical and biotechnology industries. Be it to store biological samples like cells and tissues at extremely low temperatures to preserve them for future studies to use, or even for transportation. Thus, cryo containers are part of the cold chain and therefore must be qualified and validated according to EU GDP (European Union Good Distribution Practice). These guidelines were developed to ensure the quality of pharmaceuticals throughout the entire distribution process from manufacturing to consumption.
Mar 11, 2024
The calibration of the systems and sensors currently in use, along with the complete elimination of identified deviations, constitute fundamental components of a qualification. These are essential for the subsequent validation of a critical process within a GxP context.
Feb 26, 2024
For quite some time, the question of whether to use a wired data recorder or a wireless battery-powered data logger for the validation of thermal processes in the GxP environment has been discussed.
Feb 15, 2024
In today's blog post, we would like to take you on a journey through time to the origins of Kaye and the company's early steps in the field of validating thermal processes in the pharmaceutical and biotechnological industry.
Feb 01, 2024
EN-285 is a European standard that sets guidelines for the sterilization of medical devices in healthcare facilities. When a person is expected to use EN-285 in a regulatory sense, they are required to adhere to the specific procedures and requirements outlined in the standard to ensure the effective sterilization of medical equipment.