Custom Bioaerosol Testing Protocols for Air Cleaning Technologies
At Airmid Healthgroup, we specialise in developing customised, real-world testing protocols for air cleaning technologies targeting infectious aerosols, viruses, bacteria, mould, allergens, and other fine particles.
As the world’s leading authority on indoor aerobiology, we support innovators and product teams with independent, credible data to help validate performance claims, meet regulatory requirements, and drive commercial success.
Why Choose Airmid for Custom Bioaerosol Protocol Testing?
World-Class Aerobiology Expertise
Our scientists are pioneers in bioaerosol generation, environmental chamber testing, and infectious aerosol research — bringing decades of published expertise to every project.
Tailored Testing Protocols
Every protocol is custom-built around your product’s unique claims, use-case, and performance goals — not a one-size-fits-all approach.
Marketing, QA & Regulatory Alignment
We understand what regulators, buyers, and stakeholders need to see — so you get data that works across your marketing, QA, and regulatory teams simultaneously.
Real-World Environmental Simulation
Our state-of-the-art test chambers model airflows and conditions found in homes, offices, hospitals, and schools — delivering data that reflects genuine product performance.
Agile, Confidential & Reliable
Our process is designed to move at your pace, protect your IP, and deliver clear, actionable insights on time and within budget.
Who We Help
We work with teams across the full product lifecycle:
- Product Innovators — seeking validation for new air cleaning concepts
- Product Development Managers — requiring rigorous data to advance prototypes
- Quality Assurance Specialists — who need robust test methods for internal benchmarks
- Regulatory Affairs Teams — preparing submissions for EPA, FDA, CE, or ISO compliance
- Product Marketing Managers — who need defensible claims for launch and positioning
- Sales Managers — who want scientific evidence to win deals and open new markets
Common Custom Bioaerosol Protocol Applications
- Efficacy testing for portable air purifiers including virus testing
- Performance claims for HVAC and ventilation systems against airborne pathogens
- Validation of UVGI, plasma, ionisation, or electrostatic technologies
- Allergen, mould spore, virus, and fine particle filtration and capture
- Surface and airborne pathogen reduction testing including SARS-CoV-2, Influenza, and RSV
Download a Sample Report
See an example of the quality and depth of reporting Airmid provides. Download our H1N1 sample report below:
The Airmid TTS-OTS™ Approach: To The Shelf, Off The Shelf
At Airmid, our “To The Shelf, Off The Shelf” approach is designed to complement structured innovation and product development methodologies — including Stage-Gate®, Technology Readiness Levels (TRL), and TRIZ. Whether you’re accelerating early R&D, validating prototypes, or preparing for commercial launch, our testing protocols integrate seamlessly into your innovation workflow.
Prove Performance. Win Trust. Accelerate Commercialisation.
Whether you’re preparing for a product launch, entering a new market, or seeking regulatory approval, we’ll help you generate the high-quality, defensible data you need to succeed.
Frequently Asked Questions
What is a custom bioaerosol protocol and when do I need one?
A custom bioaerosol protocol is a bespoke testing programme designed specifically around your product’s technology, claims, and target application. You need one when your product doesn’t fit neatly into a single existing standard, uses a novel technology such as plasma or ionisation, or requires testing that reflects specific real-world environments like hospitals, schools, or homes.
What air cleaning technologies can be tested using custom protocols?
Airmid can develop custom protocols for virtually any air cleaning technology including HEPA and ULPA filtration, UV-C disinfection, photocatalytic oxidation, plasma and ionisation systems, electrostatic precipitation, and combination technologies. We can also test against specific pathogens including SARS-CoV-2, Influenza, RSV, and others.
Will data from a custom protocol be accepted by regulators?
Yes — provided the study is well-designed and conducted in an accredited facility. Airmid’s GLP-compliant, ISO/IEC 17025-accredited laboratory produces data accepted by the EPA, FDA, CE marking bodies, and ISO compliance programmes. We design every custom protocol with regulatory acceptance in mind from the outset.
Can Airmid test early-stage prototypes?
Yes. We regularly work with product teams at the prototype and early R&D stage to generate proof-of-concept data, identify performance gaps, and inform design improvements — helping you de-risk development before full-scale production.
How long does a custom bioaerosol testing project take?
Timelines vary depending on the complexity of the protocol, the number of test conditions, and sample availability. Simple custom studies may be completed in 4–6 weeks, while multi-phase or multi-pathogen projects may take longer. We provide a clear timeline and cost proposal before any work begins.
Related Tests
- AHAM AC-5 Testing — Microbial CADR Certification
- ASHRAE 185.1-2020 — UV-C Disinfection in Air-Handling Units
- Substantiating Health Claims Through Scientific Research & Certification
Related Resources
- ASHRAE Standard 241: Control of Infectious Aerosols — Understanding its Impact
- Reflections on the ASHRAE Winter Meeting: Infectious Aerosols, Standard 241, and Healthy Buildings
- Understanding MERV, HEPA, and ASHRAE Standards
