GMPF P RF Real-Time Temperature & Pressure Logger for Pharmaceuticals
Simultaneously records pressure and temperature. Contributes to quality control in pharmaceutical manufacturing.
In the pharmaceutical industry, temperature management during the manufacturing process is crucial to ensure product quality and safety. In particular, temperature fluctuations during sterilization processes and storage environments can affect the efficacy and stability of products. GMPF P RF records temperature and pressure in real-time, addressing the challenges of temperature management in pharmaceutical manufacturing. 【Application Scenarios】 * Temperature measurement in autoclaves, tunnel sterilizers, freezers, refrigerators, and freeze dryers * Monitoring of temperature and pressure during the manufacturing process * Acquisition of recorded data for quality control 【Benefits of Implementation】 * Quality assurance through accurate recording of temperature and pressure * Data management with FDA 21 CFR Part 11 compliant software * Efficient operation through remote control
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basic information
**Features** * Measurement data is transferred in real-time to the dedicated software XpertLog. * ITS-90 calibration coefficients are stored in internal memory. * The software complies with FDA 21 CFR Part 11. * Network compatible: multiple users, centralized management, server database, etc. * Remote activation feature to start the logger. **Our Strengths** Lives International has been providing high-performance sterilization validation and mapping temperature measurement systems to pharmaceutical manufacturers worldwide for over 20 years. We maximize support for our customers' validation through calibration and help desk services at our domestic technical base, as well as enhanced after-sales service.
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Company information
Lives International has been providing high-performance sterilization validation and mapping temperature measurement systems to pharmaceutical manufacturers around the world for over 20 years since its establishment in France in 1998. In 2021, we opened a domestic technical base in Osaka and began regular calibration of data loggers and thermocouple systems, as well as help desk services in Japan. Moving forward, we will continue to enhance our after-sales services, including repairs, to fully support our customers' validation needs. Our research and development team is dedicated to designing products that reflect trends in the pharmaceutical industry and our customers' requests, striving daily to improve product quality. We also offer customization options. If you have any concerns regarding sterilization validation or temperature mapping, please feel free to reach out to us.
