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 12-T100-EX
Enregistreur de données de température polyvalent
Robust temperature data logger for regular independent measurements, even in hazardous areas.
EBI 12-TP231
Enregistreur de validation
highliy accurate data logger to measure temperature and pressure
EBI 12-T441-EX
Enregistreur de validation pour la mesure même en zone Ex
bendable sensor for placement in cavities
EBI 11-T240
Enregistreur de validation avec temps de réponse rapide
Validation logger with fast response time for use where space is limited
EBI 11-T231
Enregistreur de données robuste pour le contrôle des échantillons
Robust temperature data logger for process validation of production processes.
EBI 12-T102
Enregistreur de glace carbonique pour la mesure à -80 °C
Temperature measurement of up to 100 hours in dry ice.
EBI 12-T222
Enregistreur de validation polyvalent
For final inspection after the repair, but also for validation.
EBI 11-T236
Enregistreur de validation de température
Validation logger for temperature measurement in the doctors surgeries
