This webinar describes the basic concept of a dedicated pharmaceutical cleanroom monitoring system (FMS) in comparison with other, multi-application systems such as Building Management Systems (BMS), with clear pros and cons.
Differences between computer-based and industrial designed FMS will be discussed, with a focus on system reliability and data integrity aspects.
Additionally, pharmaceutical users will get a “knowledge toolkit” to ensure technical, regulatory, and quality requirements insights to ensure a proper facility monitoring system design, maximize ROI and ensure regulatory acceptance.
In this webinar you’ll learn:
- the main differences between a dedicated cleanroom FMS and BMS;
- The must-have design to be ready for the digital transformation
what to expect from regulatory changes and pharmaceutical industry trends.