Validación de los procesos de esterilización
Sterilization processes, such as steam sterilization, depyrogenation or hot air sterilization, are an important part of the manufacture of pharmaceuticals. They are designed to minimize risks to the patient. To ensure the quality of these processes, they must be both initially validated and revalidated at regular intervals.
Our highly accurate and robust validation loggers of the EBI-11 and EBI-12 family support you in this task with logger designs adapted to all operating environments. With the professional Winlog.validation, the loggers can not only be programmed and read out in an FDA-compliant manner, but it also enables an automatic evaluation of the sterilization processes. In addition, our competent and experienced staff is at your disposal for the creation of specific templates.
EBI 12-T100-EX
Registrador de datos de temperatura versátil
Robust temperature data logger for regular independent measurements, even in hazardous areas.
EBI 12-TP231
Registrador de validación
highliy accurate data logger to measure temperature and pressure
EBI 11-T240
Registrador de validación con tiempo de respuesta rápido
Validation logger with fast response time for use where space is limited
EBI 11-T231
Robusto registrador de datos para el control de muestras
Robust temperature data logger for process validation of production processes.
EBI 12-T441
Registrador de validación para mediciones en el esterilizador de vapor
bendable sensor for placement in cavities
EBI 11-T233
Robusto registrador de datos para el control de muestras
Robust temperature data logger for process validation of production processes.
EBI 12-T102
Registrador de hielo seco para medir a -80 °C
Temperature measurement of up to 100 hours in dry ice.
EBI 12-T222
Registrador de validación versátil
For final inspection after the repair, but also for validation.
EBI 11-T236
Registrador de validación de temperatura
Validation logger for temperature measurement in the doctors surgeries