LN2 Comparator

The Liquid Nitrogen (LN2) Comparator is an easy-to-use device that allows for calibrations that need extremely low temperatures. Using the boiling point of liquid nitrogen, this comparator allows you to complete calibrations at -196 C in a semi-automated fashion in combination with Kaye Validators. 

Kaye ValProbe RT Humidity/Temperature Logger

The ValProbe RT logger with humidity and temperature sensors comes with RF technology to give users real-time data viewable on their Validation Console. With a humidity range of 15% to 95%, and a temperature range from 0°C to 70°C, this logger has a wide range of capabilities for temperature and humidity mappings.

Common Reporting Tool

The Common Reporting Tool software is a comprehensive reporting utility that can be installed on a separate Windows 10 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. 

Kaye LabWatch^® IoT

The LabWatch IoT Cloud environmental monitoring system is a complete solution for critical stability, environmental, and facility monitoring applications. LabWatch IoT connects to your sites through secure VPN, detects alarm conditions and alerts personnel wherever they are, documents any number of chambers without generating stacks of paper, protects data with secure Cloud storage, and lets you access data easily for analysis. 

When assessing the effectiveness of a sterilization process, calculating the lethality using the F0 method is crucial. One significant consideration in this calculation is the duration required to eliminate a specific number of microorganisms, which can be expressed in either minutes or seconds. Using expressing time in minutes is more widely accepted and practical, understanding the differences and implications of using seconds is also important in certain scenarios. In this blog post, we'll explore the significance of expressing time in minutes or seconds when calculating lethality using the F0 method.

In industries such as healthcare, pharmaceuticals, and food processing, the use of sterile products is essential for preventing the spread of harmful microorganisms. Thermal validation is a process used to ensure that sterilization processes are capable of achieving the desired level of sterilization. This process involves exposing a product or material to a sterilization process and then testing for the presence of viable microorganisms.

Recently we presented you with information pertaining to data security and what Kaye is doing to keep your data safe. Continuing with this same topic area, there is another principle dealing with data when it comes to our Cloud-based systems. In this post, we are discussing GxP Compliance.

Unlike your car, validation and calibration equipment don’t necessarily need an oil change or their tires rotated, but there are important preventative steps you can take to help extend the life of your instruments and minimize risks for your Validation studies.

When the topic of sustainability gets brought up, often the attention is drawn to points like recycling and reducing waste. But there is so much more to it. There is no question that recycling and reusing waste products play a big role when it comes to environmental sustainability, but so too does eliminating CO2 emissions to reduce our carbon footprint. The goal of these efforts is to reduce the impact an organization has on the earth and all those that live on it. Kaye is expanding its sustainability efforts by challenging the entire organization to identify efforts that could be improved.