White Paper — Sponsored Content

Changing to the New Normal with Fully Integrated Environmental Monitoring Systems

Changing to the New Normal with Fully Integrated Environmental Monitoring Systems

Vital information for the most critical component in your cleanroom.

The manufacturing of pharmaceuticals must occur in a cleanroom. A critical component of a cleanroom is a building management system (BMS). A BMS controls the environment and personnel/material flow so that cleanroom conditions are properly maintained. For the cleanroom and the products made in them to be cGMP compliant, environmental monitoring is also required. An environmental monitoring system (EMS) ensures that the critical environmental conditions in the cleanroom, such as temperature, pressure and humidity are tracked during the operation of the cleanroom.

Routinely, environmental monitoring systems are designed and built by a separate contractor than the one who built the cleanroom. And that system is qualified after completion of a cleanroom. This practice adds unnecessary installation and testing time to the final qualification schedule of the cleanroom project. A separate EMS can also cause unnecessary issues because of extra hardware and components needed for integration of separate controllers.

With prefabricated cleanrooms, the EMS can be designed and installed during cleanroom construction by the cleanroom provider. Moreover, the environmental monitoring system (EMS) can be automated meaning that critical data including sensor readings, alarms, Audit Trail, and user access are logged and historized without additional user actions.


GCON


This paper will discuss the benefits of a fully integrated environmental monitoring system.

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