Airmid Healthgroup provides cleaning products efficacy testing services, delivering ISO 17025-accredited, GLP-compliant testing for household and commercial cleaning products — validating antimicrobial efficacy, allergen removal performance, VOC emissions, and surface safety under real-world simulated conditions. Whether you need third-party data for regulatory approval, retailer compliance, or marketing claims, our science-backed testing gives your product a defensible evidential foundation.
GLP Methods
AAFA Certification Partner
EU BPR & EPA Experience
Key cleaning product testing capabilities
Antimicrobial efficacy testing
Antimicrobial efficacy testing demonstrates that a cleaning or disinfectant product reduces microbial populations to a measurable, reproducible standard. At Airmid Healthgroup we test against bacteria, viruses (including human coronavirus surrogates), moulds, and yeasts using ASTM E1153, ASTM E1053, EN 13697, and custom client protocols. Results are reported as log reductions or percent kill rates, formatted to support manufacturer claims, retailer compliance, and regulatory submission to the EPA, ECHA, and other authorities. Studies destined for federal submission are conducted under GLP.
- → ASTM E1153, EN 13697, ASTM E1053, and custom protocols
- → Testing against bacteria, viruses (including human coronavirus), moulds, and yeasts
- → Supports “kills X%” and hospital-grade disinfectant claims
Allergen removal performance
Cleaning products marketed to allergy-sensitive consumers need defensible evidence that they actually remove allergens — not just dust. We perform allergen-removal testing using simulated real-world conditions for dust mite, pet dander, pollen, and mould allergens on hard floors, countertops, soft furnishings, and textiles. Results support certifications such as Asthma & Allergy Friendly® and credible label claims including “reduces dust mite allergens” or “allergy-friendly formula”.
- → Simulated real-world conditions for dust mite, pet dander, pollen, and mould allergens
- → Surface wipe-down efficacy on hard floors, countertops, and soft furnishings
- → Data supporting Asthma & Allergy Friendly® and similar certifications
VOC & indoor air quality impact
Cleaning products affect more than the surfaces they touch — many emit volatile organic compounds (VOCs) into the indoor air during and after application. We measure VOC emissions in real time using ISO 16000 series methods inside our environmental chambers, capturing both peak emission profiles and post-application decay. This data substantiates claims such as “low emission”, “fragrance-free”, or “non-toxic”, and aligns with green building certifications including LEED, WELL, and BREEAM.
- → VOC emissions testing using ISO 16000 series and IAQ protocols
- → Real-time measurement of gases emitted post-application
- → Substantiates “low emission,” “fragrance-free,” and “non-toxic” claims
Residue & surface safety evaluation
Beyond efficacy, cleaning products need to leave surfaces safe and intact for repeat use. Our surface compatibility evaluations cover staining, corrosion, film build-up, and contact irritation across plastics, metals, wood, textiles, and other substrates. We also assess residual antimicrobial activity, the potential for re-aerosolised allergens, and the long-term effect of repeated application — data that’s useful for product development decisions as much as for marketing claims.
- → Surface compatibility with plastics, metals, wood, and textiles
- → Evaluation of staining, corrosion, film buildup, and contact irritation
- → Assessment of residual activity and potential allergen re-exposure
Why choose Airmid for cleaning product testing?
- → ISO 17025-accredited with specialist bioaerosol, microbiology, and IAQ labs
- → Custom aerobiology exposure chambers simulating homes and public spaces
- → Experience supporting EU Biocidal Products Regulation (BPR) and EPA/FDA requirements
- → Scientific rigour with actionable commercial insight for claims and launch
Applications
- → Product claims substantiation for antimicrobial or allergen removal claims
- → Support for 510(k) filings, BPR dossiers, and EPA submissions
- → Pre-market data for label claims, green certifications, and retailer compliance
- → Comparative studies supporting product reformulation, branding, or private label claims
Airmid Healthgroup · Cleaning Product Testing
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Speak to an expert about your testing requirements or request a custom proposal.
Frequently Asked Questions
Q: How long does cleaning product efficacy testing take?
A: Typical timelines run 3 to 6 weeks from sample receipt to final report for a single test method. Larger projects covering multiple categories (antimicrobial plus allergen plus VOC, for example) usually run 6 to 10 weeks because the studies share sample preparation but each method has its own analytical workflow. We confirm timelines as part of the initial scoping call.
Q: What samples do you need from us?
A: For antimicrobial and surface safety testing we typically request enough product for triplicate runs at the recommended use concentration plus retains. For allergen and VOC testing the volumes are similar; we confirm exact quantities and packaging during scoping. Samples should arrive in their final commercial formulation and packaging where possible.
Q: Are your reports accepted by the EPA, FDA, and ECHA?
A: Our laboratory operates in conformity with ISO/IEC 17025 for accredited methods and follows GLP for studies destined for federal regulatory submission. Reports are structured to support submission, but final acceptance always rests with the receiving regulator. We can coordinate directly with your regulatory team on the report format.
Q: Can you support label claim sign-off?
A: Yes. We routinely review proposed claim language alongside the underlying test data to flag claims that aren’t supported by the study, claims that need stronger qualifiers, and claims that may attract regulator scrutiny. This is part of our advisory service rather than a separate study.
Q: Can you test against specific pathogens?
A: Yes. Our virology and microbiology labs work with bacterial (Gram-positive and Gram-negative), viral (including human coronavirus surrogates), fungal, and allergen challenges. For specific organism requests — for example, a target species named in a customer’s claim — we confirm during scoping whether the organism is in our standard repertoire or needs to be added.
Q: How do I get a quote?
A: Submit the enquiry form on this page or contact our team directly. We’ll arrange a 30-minute scoping call to discuss your test objectives, applicable standards, and timeline, then issue a written quote within 5 working days.
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