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How it Works
Disease control was never a profit center. Â Until now.


Discover the CLEANBarrier
TM
Facility-installed, 3-phase pathogen and odor control system that delivers exceptional results every day

Mold
Bacteria
Biofilm
Mycotoxins
Viruses
Odor
How it works

Surfaces
Hard, non-porous surfaces are breeding grounds for disease. Daily treatment with an EPA-registered sanitizer is the gold standard for GMP facilities.

Water

Air
Eliminate odor causing compounds “at source,” not just trapping. Reduces olfactory sensitization and improves AQ and working conditions for staff.
Eradicate waterborne disease and flow-reducing biofilm and keep it maintenance free. Plant quality thrives with truly clean water while teams are unburdened from fertigation issues.


The Platform
The CLEANBarrier in Action



PATHox
TM
surface
EPA-registered (#73139-1), no-rinse liquid sanitizer for daily use on hard non-porous surfaces (floors, walls, tables)
TM
FERTox
water
PATHox is direct-injected into fertigation system to disinfect and eliminate biofilm and pathogens
AIRRox
TM
air
Separately labelled, controlled-release deodorizing gas for daily control of odor-causing compounds & certain VOCs
Why CLEANTheory
Why CLEANTheory
Put our expertise to work. Get more out of your resources than ever before.
Safe and Easy to Use
Custom platform design and a unique chemistry means safer and more efficient working conditions for staff

Safe for plants, people, and building materials (see label for details)

Eliminate staff exposure to long-term, unhealthy levels of mold, mildew

Fewer work-related injuries/illness means increased productivity

Using an EPA-registered, high-efficacy "no-rinse sanitizer" reduces need for harsh chemicals

No "tag out" and non skin-sensitizing formula means more comfortable work environment for staff

Full system automation reduces best practices/GMP sanitation labor by up to 95%



High ROI
Using CLEANTheory every day typically results in net new profits within the first use cycle

Increased yields

Higher water quality: control pathogens/biofilm

Pass more microbial tests w/o remediation

Higher total TAC
(if medicinals)

Greater inventory control

More efficient labor for hygiene best practices

Higher throughput to market

Lower overall operational risk
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