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 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.
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.
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.
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.
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.
In the pharmaceutical industry, thorough and accurate documentation is vital when validating measurement systems. Efficiency enhancement and compliance assurance are achieved through comprehensive validation documentation and user support, as provided by Kaye Measurement Systems. This detailed documentation not only ensures regulatory compliance and enables traceability but also forms the basis for continuous improvement processes and the identification of optimization potential within the systems.
Checking the calibration parameters in data loggers is an important part of functional quality management. Especially with temperature data loggers, regular verification of the validity of the calibration data is a recommended practice within risk assessment. Mobile data loggers are exposed to various stresses that can have a lasting negative effect on the calibration offsets stored in the loggers. Documented and regularly conducted checks serve to prevent incorrect measurements and the potentially associated need to repeat an already carried out validation study.
At Kaye, a subsidiary of Amphenol, we are excited to share a significant update in our commitment to sustainability and renewable energy. With the installation of a 40 kVA solar system at our Pforzheim location in Germany, we will be able to cover more than 20% of our annual electricity consumption exclusively with self-generated solar power in the future.
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.
Launch of Kaye Validator 2000 Wired Validation System; Major re-design of current Kaye Validation systems addressing 21 CFR part 11 compliance as well as switch from paper to software based System.
