Our physician-led multidisciplinary team includes scientists with expertise in virology, bacteriology, mycology and allergy. We deliver data of impeccable quality — and we interpret results with specific regard to their likely impact on the indoor environment and people’s health.
As a world-leading testing laboratory, our data differentiates you from your competitors
No matter what your product or service life-cycle stage, we have the expertise to add value through:
- Creating modelled indoor environments with aerobiology environmental test chambers
- Ability to link chambers for complex real-world exposure scenarios
- Airborne sampling expertise across allergens, viruses, bacteria, mould, and particles
- Expertise in a broad range of analytical techniques
- Contract research and field studies
- Comprehensive, audit-ready test reports
- Reputational and accreditation benefits for clients
Consumer Products & Services
Manufacturers of consumer products face growing pressure to substantiate health and environmental claims before going to market. We work as a specialist extension to your own R&D capabilities, delivering independent scientific evidence that stands up to retailer and regulatory scrutiny.
- We enable innovation by stimulating ideas and complementing your R&D efforts
- We understand the importance of speed and meeting commercial deadlines
- We help you manage reputational issues, insurance risk, and regulatory compliance
Indoor Environments
For building materials, HVAC systems, and indoor environment technologies, we provide robust scientific evidence linking product performance to occupant health outcomes.
- Environmental data capture for health-related parameters
- Health-related environmental trials and real-world field studies
- Epidemiology studies where bio-monitoring and human exposure assessments are required
Our Facility
Our large aerobiology environmental test chambers and state-of-the-art analytical technology measure multiple parameters related to indoor air quality simultaneously. Clients regularly describe Airmid as a specialised extension of their own research capabilities.
Biological
Viruses, Bacteria & Mould
Aerosolised and surface pathogen measurement in controlled environments
Allergens
Allergen Quantification
Airborne and settled allergen levels using ISO 17025-accredited methods
Particles
PM2.5, PM10 & Ultrafine
Indoor air pollutants including toxins and ultrafine particle measurement
Why Independent Claims Verification Matters
Today’s consumers are constantly in search of the newest product trends. While innovation and time to market are key to success, safety, correct labelling, and compliance are equally important. Retailers are increasingly risk-averse and wish to protect their brand reputation.
Asthma, allergy, and health-related labelling claims, as well as ingredient listings and marketing materials, are becoming more tightly regulated. The best way to substantiate a claim is through independent third-party testing. It is vital with any new product innovation that all necessary claims are verified and substantiated prior to going to market.
We can diagnose existing approaches, design new strategies to drive innovation, and help you enhance the quality and reputation of your organisation — while avoiding risk. Our services help you with:
Accelerated innovation cycles and reduced R&D costs
Faster time to market for prototypes and new product launches
Reputational protection, insurance confidence, and risk mitigation
Environmental data capture and health-related field studies and bio-monitoring
Accreditation & Compliance
Airmid Healthgroup is ISO 17025-accredited and offers high-quality testing, inspection, compliance and certification aligned with several regulatory systems. Our labs are routinely and externally audited to ensure that your data is reliable, repeatable, and scientifically accurate. We meet the requirements for submission to both the US EPA and the US FDA. Whether you are in early R&D or require GLP testing for a 510(k) submission, contact us with your testing needs.
Good Laboratory Practices (GLP)
Good Laboratory Practices were enacted as law in 1978 to ensure that all data submitted to federal regulatory agencies is performed safely and reliably. The GLPs assure that a study is conducted by qualified personnel working in well-maintained facilities with appropriate materials and calibrated equipment, using properly designed experiments recorded with clear and complete detailed documentation, overseen by an independent Quality Assurance Unit, and safely archived for audit and inspection by regulatory agents.
EPA GLP
EPA Good Laboratory Practices ensure the quality and integrity of test data submitted to the Environmental Protection Agency. The EPA writes regulations, provides guidance, reviews submitted data, inspects for compliance, registers toxic materials, and enforces legal action for violations.
FDA GLP
FDA GLP prescribes good laboratory practices for conducting nonclinical laboratory studies that support or are intended to support applications for research or marketing permits for products regulated by the Food and Drug Administration. At Airmid Healthgroup, all testing services are conducted in strict accordance with FDA and EPA guidelines and cGLP regulations — ensuring clients receive results that are both reliable and recognised by regulatory bodies.
Ready to verify your health-based claims?
Contact our team to discuss your testing requirements and receive a tailored proposal.
