• ePASE® module offers the ease of validating and compounding of support and antineoplastic treatments, following the guidelines established in GMP.

  • ePASE® enables to simultaneously determine the substance (drug) that should be added to a preparation (parenteral mixture) and its quantity, through a qualitative and quantitative monitoring (precision scale for gravimetric control). ePase® is an intuitive handling tool, as it has a guidance screen that helps the user with every step of the process.

  • It enables real time monitoring of every step in the process taking place in the biological safety cabinet, by means of tele-validation.

  • Facilitates to professionals involved in compounding parental admixtures the control of occupational exposure risk.

  • It offers predefined or configurable high-value statistics for the continuous improvement of assistance quality and patient safety.

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