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FrançaisProbiotic Cleaning for Cleanrooms & Controlled Environments
Sanitify probiotic cleaner uses live Bacillus ferment to establish competitive microbial control on cleanroom surfaces — reducing bioburden without chemical residues, VOC emissions, or corrosion risk to sensitive equipment and production materials.
Why Probiotic Biofilm Control Outperforms Chemical-Only Cleanroom Protocols
Chemical disinfectants in cleanrooms create a paradox: they achieve momentary sterility but leave surfaces immediately vulnerable to recontamination. Sanitify introduces non-pathogenic Bacillus bacteria that occupy surface niches, consume organic nutrients, and form a protective biofilm — continuously suppressing pathogenic colonisation for up to 72 hours. This reduces the bioburden recovery rate between cleaning cycles by 70–90% compared to chemical-only protocols.
Sanitify does not generate particles, VOCs, or outgassing. It can be used in ISO 14644-classified environments as part of a validated cleaning protocol. Facilities should validate through standard IQ/OQ/PQ procedures for their specific classification requirements.
No — Bacillus spores are applied to surfaces and remain surface-bound. They do not generate airborne particles or VOCs. Environmental monitoring data from validated installations shows no impact on air quality metrics.
Yes — Sanitify is designed as a complementary layer. Apply after primary chemical disinfection to establish biological contamination suppression during the inter-clean period. It does not chemically interact with standard cleanroom disinfectants.
No — Sanitify leaves zero chemical residue. The Bacillus bacteria form a microscopic biofilm that does not produce visible, chemical, or particulate residue. It will not contaminate pharmaceutical, semiconductor, or food production processes.
Sanitify can be incorporated into GMP-documented cleaning procedures. It does not replace validated disinfection steps but provides documented biological contamination suppression between cycles. Full documentation and certificates of analysis are available for quality system integration.
Apply, Establish, Maintain — Continuous Microbial Suppression
Apply Sanitify to cleanroom surfaces — stainless steel work surfaces, laminar flow hoods, pass-through chambers, gowning area benches, walls, and flooring. The probiotic formula leaves zero chemical residue and requires no rinse cycle. Bacillus spores germinate within minutes and begin establishing competitive dominance, maintaining microbial suppression throughout operational periods.
What our customers are saying?
Zero Residue, Zero VOCs — Safe for Sensitive Production
Traditional cleanroom disinfectants (quaternary ammonium, peracetic acid, hydrogen peroxide, isopropyl alcohol) provide instant kill but zero residual protection. Surfaces are sterile for seconds, then immediately susceptible to airborne and personnel-transferred contamination. Sanitify fills this gap by maintaining a living biological barrier. The Bacillus biofilm does not produce particles, VOCs, or outgassing — critical factors in ISO 14644-class environments where air quality and surface chemistry are tightly regulated.
No volatile organic compounds (VOCs) — no impact on air quality monitoring or personnel health. No corrosive agents — safe for stainless steel, polycarbonate, HEPA filter housings, and sensitive electronics. No residue that could contaminate production materials, pharmaceutical intermediates, or semiconductor wafers. Compatible with existing cleanroom qualification procedures (IQ/OQ/PQ) and GMP documentation requirements.
The Science: Bacillus Competitive Exclusion in Controlled Environments
Sanitify contains Bacillus subtilis and Bacillus amyloliquefaciens spores — Biosafety Level 1 organisms that are non-pathogenic, non-toxigenic, and do not produce endotoxins at levels relevant to cleanroom standards. These bacteria produce lipase, protease, and surfactin — bioactive compounds that disrupt pathogenic biofilm formation, degrade organic residues, and competitively exclude contaminant organisms. In validated trials, probiotic surface treatment maintained significantly lower aerobic colony counts over 48–72 hours compared to chemical disinfection alone.
Cleanroom Applications
Pharmaceutical cleanrooms (ISO 5–8): Surface bioburden control between validated cleaning cycles | Semiconductor and electronics manufacturing: Residue-free surface maintenance for sensitive production | Biotechnology labs: Continuous biological contamination suppression | Medical device manufacturing: GMP-compatible surface microbial control | Food-grade cleanrooms: HACCP-compatible biofilm prevention | Aerospace cleanrooms: Particle-free biological surface treatment
Upgrade Your Cleanroom to Probiotic Biocontrol
Our Cleanroom Products
Universal Probiotic Cleaner
Food-safe surface cleaner with 72-hour protection for kitchens and prep areas.
Probiotic Acidic Cleaner
Specialist formula for limescale and mineral deposits on kitchen equipment.
Frequently Asked Questions About Probiotic Cleanroom Cleaning
How often should cleanrooms apply Sanitify?
Application frequency depends on cleanroom classification and operational intensity. Typical protocols: ISO 5–6 environments every 24 hours; ISO 7–8 environments every 48–72 hours. Higher-traffic zones may require more frequent application. Validate based on environmental monitoring data.
Can Sanitify be used in pharmaceutical manufacturing?
Yes — Sanitify organisms are Biosafety Level 1, non-pathogenic, and do not produce endotoxins at relevant levels. It is suitable for pharmaceutical facility surface treatment as part of a validated, documented cleaning protocol.
How does Sanitify compare to hydrogen peroxide vapour (HPV)?
HPV provides excellent whole-room decontamination but requires room evacuation, lengthy aeration, and offers no residual protection. Sanitify provides 48–72 hours of surface-level biological suppression with no room downtime. Many facilities combine HPV for periodic decontamination with Sanitify for continuous inter-clean protection.
Will Sanitify interfere with environmental monitoring?
Bacillus subtilis and B. amyloliquefaciens are readily identifiable in environmental monitoring programs. They are recognized non-pathogenic organisms and can be documented in trending data as part of the probiotic cleaning protocol. They do not mask or interfere with detection of pathogenic organisms.
What validation documentation is available?
Sanitify provides certificates of analysis, safety data sheets, product stability data, and antimicrobial efficacy test reports. These documents support integration into IQ/OQ/PQ validation protocols and GMP documentation packages. Contact our technical team for facility-specific validation support.
Can Sanitify be used in semiconductor cleanrooms?
Yes — Sanitify is residue-free and does not generate particulates or outgas VOCs. It is suitable for surface maintenance in semiconductor fabrication environments where chemical residue contamination is a critical concern.
Is probiotic cleaning certified for cleanroom use?
Sanitify products are REACH-registered and comply with the EU Biocidal Products Regulation. The active organisms are Biosafety Level 1. Cleanroom certification is facility-specific — facilities should validate through their own qualification procedures.
Does Sanitify have an odour?
Sanitify is fragrance-free and produces no detectable VOCs. There may be a very faint earthy note for 1–2 minutes as spores activate — this is below detection thresholds for standard cleanroom air monitoring.
What is the shelf life?
24 months from production date when stored at 15–25°C away from direct sunlight. Once opened, use within 12 months for optimal spore viability. Store in standard cleanroom supply areas — no refrigeration required.
How should Sanitify be introduced to an existing cleanroom protocol?
We recommend a phased approach: (1) baseline environmental monitoring, (2) pilot application in a defined zone, (3) post-application monitoring comparison, (4) protocol documentation and SOP update, (5) full deployment. Our technical team provides support throughout the validation process.
Where can we purchase Sanitify for our facility?
Sanitify cleanroom products are available through our online shop with EU-wide delivery in 2–5 business days. Volume pricing, technical consultation, and validation support packages are available for cleanroom facilities. Contact our B2B team for institutional quotes.
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