GMP-compliant operation for pharmaceutical production areas

GMP-compliant operation requires reliable airborne germ monitoring. A permanently installed airborne germ monitoring system offers major advantages over mobile air samplers in class A and B clean rooms.

High reproducibility, minimal interruptions to the production process with a high degree of operational reliability, simple integration into the machine’s own HMI including integration into a parent process control system, standard quality-relevant analyses: asip compact combines all the requirements for GMP-compliant airborne germ procedures in a pharmaceutical production facility in the smallest possible space.

Integrated control, ventilation technology and air disinfection

Benefits of asip – the integrated measurement system

Research staff press the button
  • Prevent contamination
    The risk of contamination is eliminated by avoiding the introduction of devices in the clean room. Cross-contamination by used measuring equipment is also effectively prevented.
  • High reproducibility of measuring points
    Thanks to permanently installed piping, the measuring point is always clearly defined, so the operator doesn’t have to search for a plan. This ensures high reproducibility and precision.

A close look at germs

Vacuum cleaners are not only used in people’s homes.  They are also used in clean rooms – specifically in the form of “Microbiology air sampling in process” (asip) technology. Learn how this works and to what extent pharmaceuticals companies can benefit from it.

To the magazine article

Minimal interruptions to production process

The measurement is done with fixed piping and pre-defined processes, meaning minimal interruptions to production workflows. Automatic insertion of the media plates reduces the risk of errors and contamination.

The system uses a highly reliably control that is dependable even in demanding industrial operations.

For zones with high personnel and material traffic, swivelling measuring points offer a flexible solution. These points can be moved to the zone during measurement and then swivelled back to the wall without interrupting the workflow.

The user interface has a simple and clear structure, ensuring that users are always informed about the status of the measurement. There is no longer a need for an SOP.

The permanently installed piping is automatically cleaned during cleaning and sanitising of the clean room. The touch panel can be sanitised and cleaned with all standard clean room disinfectants.

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