Infection Control & Antimicrobial Technologies Testing Services

Airmid Healthgroup provides ISO 17025-accredited, GLP-compliant testing services for antimicrobial surfaces and infection control technologies. We help manufacturers validate performance claims, support regulatory filings, and differentiate products in a competitive market — with testing methods recognised by EPA, FDA, Health Canada, and CE marking processes.

Who we help

Scientist in protective suit conducting bioaerosol sampling inside Airmid Healthgroup's EN 14476:2013 testing facility
Pathogen aerosol testing in a biosafety chamber at Airmid Healthgroup — validating infection control technologies under controlled conditions.

Our services are designed for teams at the intersection of science, product development, and regulatory compliance:

  • Product Managers and R&D Leads developing antimicrobial surface technologies, infection control systems, and healthcare products requiring validated microbial efficacy claims.
  • Regulatory Affairs and Quality Assurance Teams seeking robust test data for submissions to the EPA, FDA, Health Canada, and for CE marking.
  • Innovation Leaders in medtech, consumer electronics, HVAC, and public infrastructure integrating antimicrobial features into their products.

Antimicrobial testing services

We test a broad range of products, materials, and technologies against bacteria, fungi, and viruses under controlled laboratory conditions:

Surface & Coating Efficacy

Antimicrobial coatings, treated surfaces, and hard-surface disinfectants. Pathogen-specific evaluations against MRSA, E. coli, Staphylococcus aureus, influenza, and SARS-CoV-2.

ISO 22196 · ASTM E2149 · JIS Z 2801 · relevant EN standards

Aerosolised Pathogen Testing

Controlled chamber environments simulating real-world pathogen exposure — for hospital equipment, HVAC components, textiles, and consumer goods.

Custom exposure protocols for your specific use-case

Standards-Specific Testing

ISO 21702 · ISO 18184 · BS EN ISO 20743 · ISO 27447 · ISO 22196 · ISO 13125 · ISO 18061 · ISO 17094

All standards accepted by EPA, FDA, Health Canada & CE marking

Product development and regulatory support

Navigating the path from product development to market release involves stringent regulatory requirements. Airmid Healthgroup supports this journey with data-driven insights to inform product optimisation, and test data suitable for submissions to:

We also develop customised testing protocols aligned with specific regulatory standards and guidelines, ensuring your product meets the necessary criteria for safety and efficacy across target markets.

Why choose Airmid

State-of-the-art facilities

Aerobiology chambers and surface challenge facilities for high-fidelity testing under controlled conditions.

Scientific integrity

GLP-compliant and ISO 17025-accredited methodologies ensuring reliable, reproducible results.

Real-world relevance

Custom exposure protocols reflecting actual usage scenarios — providing meaningful data for product claims.

Multidisciplinary expertise

Microbiologists, bioaerosol scientists, and regulatory experts working together on every engagement.

Efficient processes

Fast, collaborative approach to accelerate your product’s time-to-market without compromising rigour.

Case studies

Case study

Validation of Beko’s HygieneShield™ Range

Airmid confirmed the ability of Beko’s HygieneShield™ range to eliminate up to 99.999% of bacteria and viruses using UV light and high-temperature technology.

Read case study →

Case study

Dyson Study on Hand Washing, Drying, and Indoor Air Quality

Airmid contributed scientific testing and analysis to a Dyson-commissioned study examining the relationship between hand washing, drying methods, and indoor air quality.

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Related blog posts

Ready to validate your antimicrobial claims?

Partner with Airmid Healthgroup to ensure your products meet the highest standards of safety and efficacy — from development to market.

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External resources

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