Impurity detected
Precision in Purity

Find what shouldn't be there.

Instruments for contamination control in pharmaceutical cleanrooms — with the documentation to prove it.

Validated against ✓ ISO 14644-1 ✓ EU GMP Annex 1 ✓ 21 CFR Part 11 ✓ ISO 21501-4 ✓ USP ‹1116›
Made by Omnicon

Instruments we build

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DataTOC
DATA INTEGRITY

DataTOC

On-line TOC analyzer with 21 CFR Part 11 compliance built in: e-signatures, audit trail and on-board validation.

21 CFR Part 11
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WATER ACTIVITY

Aquatada

Water activity meter with on-board standalone software built for 21 CFR compliance.

Details coming soon
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MICROBIAL MONITORING

Aeris P

Settle plate changer for Petri dishes.

Details coming soon
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Why Omnicon

Documentation your QA team can file as-is

Every instrument ships with a traceable calibration certificate, an IQ/OQ pack and the raw data behind both.

Validation services →
How we work

One partner from specification to recalibration

01

Specify

An applications engineer maps sample points to your contamination control strategy.

02

Install

Wall, isolator or RABS mounting by our own technicians, during your shutdown window.

03

Qualify

IQ/OQ executed against protocols you approve before we arrive.

04

Maintain

Annual calibration, traceable to national standards, with a loan unit on site.

Tell us about your room. We'll specify the instrument.

Grade, volume, air changes — that's enough to start.

Request a quote →