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Online UPS and isolation transformers for pharma plants

In a GMP environment a power event is not only a downtime cost — it is a deviation, an investigation and potentially a lost batch.

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About Pharmaceutical & Life Sciences. We reply within one working day.

e.g. 12 kW IT load, or 60 kVA three phase

Equipment on the circuit, backup time needed, site location, and any deadline.

+91 86686 14124
Pharmaceutical & Life Sciences — power systems supplied by Extreme Power System, Pune

What actually goes wrong

A pharmaceutical site has to prove that conditions were maintained, not just that the plant kept running. A stability chamber that drifted for twenty minutes, an HPLC run interrupted mid-sequence, a lyophiliser that lost vacuum — each generates a deviation report, and the investigation costs more than the power event did. Meanwhile the QC lab’s analysers need a noise floor that most industrial supplies cannot deliver.

Specification stage

What to get right

The decisions on this list are the ones that are expensive to change after the equipment is on site.

  • Qualification documentation

    IQ/OQ protocols and traceable calibration certificates for commissioning instruments. Ask for these at the quotation stage — retrofitting the paperwork later is painful.

  • Laboratory noise floor

    HPLC, GC-MS and spectrophotometers are microvolt-signal instruments. Ultra isolation with over 100 dB attenuation is standard specification.

  • Environmental chambers

    Stability chambers and cold rooms need continuity across the DG start window or the excursion becomes a deviation.

  • Clean room HVAC

    Differential pressure has to be maintained. AHU control supplies belong on the no-break side even when the fan motors do not.

  • Data integrity

    Under 21 CFR Part 11 expectations, servers and instrument workstations losing power mid-write is a data integrity issue, not just an IT one.

  • Audit-ready maintenance

    Preventive maintenance and battery test records get inspected. Our AMC reports are formatted to be handed over directly.

Typically specified

What we supply into this sector

Pharmaceutical & Life Sciences — questions we get asked

Anything not covered here, call us — most of it is faster to answer on the phone.

Do you provide IQ/OQ documentation for pharma installations?

Yes, on request at the quotation stage. Installation and operational qualification protocols, calibration certificates traceable to national standards for the test instruments, and commissioning records in a format that goes into your validation file. It needs to be scoped up front, not added afterwards.

Which pharma loads should be on UPS rather than DG?

Anything where a fifteen-second break creates a deviation: stability chambers, environmental monitoring, instrument workstations and servers, clean room pressure control, and any process mid-cycle such as a lyophiliser. Utilities and general lighting can sit on the DG side.

We will do the load grading with you

Site survey, load list and a single-line diagram before anything is quoted. That is where the specification is actually decided.

Book a survey

Request a quote

About Pharmaceutical & Life Sciences enquiry. We reply within one working day.

e.g. 12 kW IT load, or 60 kVA three phase

Equipment on the circuit, backup time needed, site location, and any deadline.

Call
Reply within one working daySite survey before anything above 20 kVAAny make serviced