Validation des processus de stérilisation
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
Enregistreur de données robuste
Robust temperature data logger for process validation of production processes.
EBI 11-T240
Enregistreur de validation avec temps de réponse rapide
Validation logger with fast response time for use where space is limited
EBI 12-TP231
Enregistreur de validation
highliy accurate data logger to measure temperature and pressure
EBI 12-TP290
Enregistreur de pression de précision
high precision pressure measurement down to 0.1 mbar
EBI 11-T236
Enregistreur de validation de température
Validation logger for temperature measurement in the doctors surgeries
EBI 12-T230
Enregistreur de température pour la pasteurisation
Robust data logger for regular checks in canning factory.
EBI 11-P111
Mini-enregistreur de pression pour la validation
Mini validation pressure data logger to messure in steam sterilizers and Washer disinfectors.
EBI 12-T222
Enregistreur de validation polyvalent
For final inspection after the repair, but also for validation.
EBI 12-T102
Enregistreur de glace carbonique pour la mesure à -80 °C
Temperature measurement of up to 100 hours in dry ice.
