Kaye ValProbe RT CO₂ Logger

The 3-in-1 data logger from the Kaye ValProbe RT product line offers the capability to measure critical parameters such as CO₂ (carbon dioxide), relative humidity (RH), and temperature with a single device. For applications where these measurements are quality-critical, the Kaye ValProbe RT CO₂ Logger provides economical, accurate, and GxP-compliant recording and documentation of these parameters.

Kaye ValProbe RT 1.3

ValProbe RT, Kaye’s industry leading wireless validation system, is ready to operate at version 1.3. This major software update implements many new features that greatly improve user experience.

Common Reporting Tool 1.4

The Common Reporting Tool is a comprehensive software compatible with Windows based PCs. It enables you to create reports from your Kaye Validator AVS or ValProbe RT Qualification study files, offering a practical solution for documenting the results of your validation studies.

Kaye LTR-200

The Kaye LTR-200 is a multi-purpose Temperature Calibrator specifically designed to address the capacity and flexibility needs for thermal validation. This essential Temperature Calibrator utilizes its ability to perform Temperature Calibration on up to 24 thermocouples capacity. Due to hybrid technology, the LTR-200 Temperature Calibrator saves hours of time and effort when calibrating or verifying validation Temperature Sensors.

Kaye ValProbe RT 5-Channel Bendable Logger

The real-time Kaye ValProbe RT data loggers, obtainable in one and two sensor versions, are now also available with five sensors in conjunction with bendable probes. The advanced electronics of the loggers in combination with the PT-1000 Sensors achieves an accuracy of up to 0.10°C and at the same time enable an extended battery life. This Logger supports up to 100,000 samples per measurement channel – so a total of up to half a million datapoints per device.

The latest expansion of the Kaye ValProbe RT® product line introduces additional technical and user-oriented features that improve user-friendliness and broaden the application spectrum for GxP compliant validation studies. Thanks to improved hardware and software features, such as the support for up to 50 Kaye ValProbe RT® real-time data loggers per study, application-centric applications such as CO2 incubator qualification are sustainably supported. An additional standard evaluation tool based on AFNOR FDX15-140 also simplifies the qualification of climatic chambers of any type and size.

The pharmaceutical industry constantly faces the challenge of meeting stringent regulatory requirements and high-quality standards. One of the essential tasks is the qualification of critical process equipment. Traditionally, predefined guidelines and standards are followed. However, the increasing focus on quality and safety necessitates more: a comprehensive risk analysis that identifies and evaluates potential sources of hazards. In this paper, we highlight why risk analysis is an indispensable part of the qualification process and how it can be effectively integrated into the qualification plan. The goal is to raise awareness and underscore the importance of risk analysis with subsequent risk evaluation.

In the meticulous environment of pharmaceutical operations, ensuring the integrity and security of data loggers is paramount. The management of Kaye ValProbe (RT) data loggers requires high-quality, robust solutions to simplify transport, storage, and management—key aspects to maintain the accuracy of crucial data.

Everyone who has ever purchased a measuring system knows this. The true quality of the supplier is not only shown in printed words on a data sheet or a favorable offer. It shows itself when it comes to essential after-sales support. Be it the annual calibration, help, and support during commissioning, training for changing operating personnel, or bridging bottlenecks in your own measuring device. Particularly attentive readers of our blog series are certainly looking forward to what Kaye has had to offer in this area from the beginning.

Isn't it familiar? Despite all precautions and a detailed validation plan, it can happen that at the beginning of the validation you realize that one or more measuring systems are outside the calibration interval or are defective. This is annoying as it usually means a delay in qualification and a delay in the planned equipment validation - with all the associated costs. An effective method to avoid such unwanted changes in planning is to secure all Kaye validation and monitoring systems through a fixed and individually tailored maintenance plan. But how can Kaye as a manufacturer assist?