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PHARMA ANDCLEAN ROOMMANUFACTURINGA regulated market where scientificdata applications are inherentlyMANUAL, EXPENSIVE and SLOW

The current process to run cleanroom batches includes . . .

PRINTING OUT DAILYMEASUREMENTS FOR EACH LOCATION.MANUALLY ENTERING THESAMPLE AMOUNTS NEEDED FOREACH RUN.PRINTING THE COLLECTED DATA.HAVING ANOTHER OPERATORCONFIRM AND SIGN OFF ON THEBATCH.

MISTAKES CANHAPPENWhich couldresult in batch reruns, dumpsand FDAcomplications

WHAT IFThere was technology thatallows for these implementations to be FASTER, more EFFICIENT and AUTOMATED ...ANDFDA READY?

The Digital Air Seriesallows operators toremotely ONBOARD,OPERATE and COLLECTscientific data frommulti-vendor particlecounter machines allfrom a single UI

In heavily regulatedIn heavily regulatedenvironmentsenvironmentsIt's mission-critical that PHARMACEUTICALS AREMANUFACTURED IN PRECISE CONDITIONS TO BEIN COMPLIANCE WITHCURRENT GOODMANUFACTURING PRACTICE REGULATIONS

The EDGMakerDigital Air Series

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