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 11-T230
Robusto registrador de datos
Robust temperature data logger for process validation of production processes.
EBI 11-T233
Robusto registrador de datos
Robust temperature data logger for process validation of production processes.
EBI 11-T240
Registrador de validación con tiempo de respuesta rápido
Validation logger with fast response time for use where space is limited
EBI 12-TP231
Registrador de validación
highliy accurate data logger to measure temperature and pressure
EBI 12-TP290
Registrador de presión de precisión
high precision pressure measurement down to 0.1 mbar
EBI 11-T236
Registrador de validación de temperatura
Validation logger for temperature measurement in the doctors surgeries
EBI 12-T230
Registrador de temperatura para la pasteurización
Robust data logger for regular checks in canning factory.
EBI 11-P111
Mini registrador de presión para validación
Mini validation pressure data logger to messure in steam sterilizers and Washer disinfectors.
EBI 12-T222
Registrador de validación versátil
For final inspection after the repair, but also for validation.