Advisory Services for Indoor Air Quality and Product Validation
At Airmid Healthgroup, we provide advisory services to support innovators in Med-Tech, Health-Tech, IAQ, IEQ, consumer health, and building science with science-backed advisory and testing services.
From product development to post-market validation, our GLP-certified testing and ISO 17025-accredited laboratories enable independent verification of health-related claims.
Using proprietary bioaerosol exposure chambers, we assess antimicrobial efficacy, airborne pathogen mitigation, allergen reduction, and indoor air safety — translating complex science into actionable insights for regulatory approval, ESG compliance, and competitive advantage.
Whether its soft lines or hard lines for your product or service journey map either on your way “to the shelf” or if you are seeking market success; “off the shelf” we can support each step of that journey.
We have a proven track record in R & D; Testing, Inspection, Certification, Compliance, Verification or in-market amplification.
Please also review our “who we help” age as we have mapped our advisory services offering not only to the product development map but also specifically to the professionals who are responsible for each stage.
Research & Development Support
- Customized and standardized testing for respiratory health, allergy, and infection control products
- Scientific input to refine product design and inform regulatory positioning
- Ideal for IAQ devices, health-focused textiles, disinfectants, coatings, and HVAC innovations
Explore our Research & Development Support Services
Advisory Services for Claims Verification
- Independent performance validation for air cleaners, antimicrobial surfaces, and textiles
- Testing aligned with ISO 16000, ASTM E3135, ISO 18184, and custom protocols
- Multidisciplinary team with expertise in virology, bacteriology, mycology, and allergy science
- Results interpreted in the context of indoor air quality, occupant exposure, and human health impact
Explore our Claims Verification, Certification and Compliance Services
Policy & Government Consulting
- Institutional innovation pathways with legal and standards insight
- Engagement with regulators, trade groups, and standard-setting bodies
- 501(c)(6) aligned consulting via the iAIR Institute in Washington, D.C.
Explore our Policy & Government Consulting Services
Advisory Services for Education & Training
- Product development and launch education for internal teams
- Stakeholder training for architects, specifiers, and policy leaders
- Expert-led courses and advisory services on IAQ, infection control, and bioaerosol science
Explore our Education & Training Services
Retailer & Private Label Consulting
- Expert review of health-related claims on IAQ and antimicrobial products
- Testing and advisory services to meet internal QA thresholds
- Support navigating an increasingly litigious and unregulated product landscape
Explore our Retailer & Private Label Consulting Services
The above services are mainly focused on product development but product are ultimately deployed in a buildings so we also can follow the product out of the lab and test it in situ at offer a multitude of environmental testing services.
Advisory Services for Indoor Environmental Testing
- Testing services for hospitals, schools, transport hubs, retail spaces, and more (Public, Personal Work, travel)
- Environmental monitoring for particulates, pathogens, allergens, VOCs, and bioaerosols
- Aligns with building wellness certifications, employer ESG goals, and occupant health strategies
Explore our Indoor Environmental Testing
Related Articles
Read more on claim and verification:
Understanding MERV, HEPA, and ASHRAE Standards (Feb 27, 2025)
Written by Dr. Angela Southey PhD, MPH, this article explains MERV, HEPA, and key ASHRAE standards in the context of product testing and compliance—an ideal fit for your Claims Verification and Indoor Environmental Testing.
From Compliance to Outcomes: Airmid at ASHRAE 2025 (Jun 11, 2025)
Authored by Emma Gribben MSc at the iAIR Institute, this piece highlights Airmid’s involvement at ASHRAE 2025 and its push toward outcome‑driven IAQ standards. It reinforces your R&D and Policy & Government Consulting messaging.
Read more on our Verification and R&D Support sections
FAQ: ISO 16000‑36:2018 Testing for Air Purifiers (Mar 28, 2025)
A detailed FAQ by Oliver Dsa MSc covering the ISO 16000‑36 standard for bacterial efficacy testing in air purifiers. Perfect supporting link for both Claims
Read more on our : To the Shelf-Off the Shelf Framework (TT-SOTSTM)
From Lab Bench to Loyalty: The People Powering Health-Focused Innovation
Related Case Studies
Airmid Validates Fellowes® AeraMax™ Air Purifiers for Removing Cold and Flu Viruses
Airmid validates Fellowes® AeraMax™ air purifiers as highly effective at removing airborne influenza and cold viruses, supporting healthier indoor environments.
Mercedes-Benz USA’s cabin air filters, tested by Airmid Healthgroup, for Certification for their proven allergen and particle filtration
Tarkett FiberFloor® Achieves Certification for Healthy Indoor Air
Tarkett, a global leader in flooring solutions, partnered with Airmid Healthgroup to scientifically validate the health benefits of their FiberFloor® product line.
External Links
https://www.allergystandards.com/news_events/selfie-seals-the-perils-of-self-certification/
Helpful Word Tags
GLP testing | ISO 17025 lab | airborne pathogen testing | claims verification | bioaerosol testing | IAQ consulting | indoor air quality testing | antimicrobial efficacy | product validation | aerobiology laboratory
Key Phrases
GLP-certified testing laboratory for health claims | ISO 17025-accredited indoor air quality lab | bioaerosol chamber testing for product validation | independent claims verification for IAQ devices | antimicrobial surface testing using ISO 18184 | consulting services for IAQ and ESG compliance | custom testing protocols for airborne pathogens | R&D support for health-focused product innovation | indoor environmental testing for buildings and schools | air quality education and stakeholder training programs
Accreditation & Compliance
- iAIR Labs offers high-quality testing, inspection, compliance and certification with several regulatory systems.
- Our labs are routinely, 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’re interested in early R&D for your product or GLP testing for a 510k, contact us with your testing needs.
Good Laboratory Practices (GLP)
The 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 were introduced to 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/inspection by regulatory agents.
EPA GLP
EPA Good Laboratory Practices (GLP) ensures 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 (FDA). This program supports customers requesting a GLP assessment, as FDA does not provide a certificate of compliance.
At iAIR Labs, we pride ourselves on adhering to the highest standards of regulatory compliance. All our testing services are conducted in strict accordance with FDA and EPA guidelines and cGLP (current Good Laboratory Practice) regulations, ensuring our clients receive results that are both reliable and recognized by regulatory bodies.
