ARE Labs

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Drug Delivery

MDI, DPI, nebulizer, and nasal-spray performance per USP & EP.

MDI Inhalers DPI Inhalers Nebulizers Other Drug Delivery Nasal Spray Devices Browse all →

Air Treatment

Room air cleaners, in-line duct filtration, UV/UVGI, filter media.

In-Line Duct Systems Room Purifiers Large Air Cleaners UV / UVGI Devices Other Air Treatment Filter Media Browse all →

Spray & Aerosol

Consumer and industrial sprays, foggers, pump and pressurized formats.

Industrial Sprays Consumer Sprays Pump Sprays Oral Sprays Powder Sprays Other Pressurized Area Foggers Fire Suppression Browse all →

Respiratory

Masks, respirators, PAP devices, anesthesia systems, and breathing-pathway testing.

Masks & Respirators CPAP / BiPAP / PAP Anesthesia Machines Browse all →

Medical Devices

Sterile packaging, particle-emitting equipment, surface treatment, and bioaerosol monitors.

Sterile Packaging Particle Emissions Surface Treatment Biodetectors Browse all →

Surface & Antimicrobial

Treated hard surfaces and antimicrobial fabrics and textiles.

Hard Surfaces Fabrics & Textiles Browse all →

Case Studies

Technical project stories showing study design, anonymized data, interpretation, and product-development implications.

Cosmetic Package Integrity Dry Powder Nasal Spray First-Minute Bioaerosol School Air Purifier Study Browse all →

Success Stories

Client outcome stories showing the challenge, ARE Labs collaboration, turning point, and business or program impact.

Fragrance Aerosol Testing Glow Guardian Candle Prop 65 TiO2 Testing Browse all →

Regulatory Insights

Plain-language guidance on antimicrobial, air-purification, and claim-substantiation risk, grounded in public EPA, FTC, and federal sources.

Antimicrobial & Air-Purification Claims Browse all →

Aerosol Science

Practical explainers for aerosol behavior, particle sizing, bioaerosol generation, and test scoping.

Aerosol Science Basics Bioaerosol Generation & Sampling Spray & Plume Dynamics Understanding Particle Size Browse all →

Regulatory Guidance

Regulatory and standards context for stability, validation, documentation, and method decisions.

AHAM AC-1 / AC-5 Standards ASHRAE 241 Infection Risk Mitigation FDA Inhalation Device Guidance GLP vs. GMP: What's the Difference?ICH Q1A(R2) Stability Guidelines ISO 17025 Accreditation Explained Browse all →

Filtration

Filter ratings, gas-phase removal, room-air-cleaner claims, and performance terminology.

Gas-Phase and VOC Filtration HEPA vs. ULPA Filters MERV Ratings Explained Browse all →

Disinfection

UVGI, antimicrobial, surface, and biofilm claim context for test planning.

Antimicrobial Testing Methods Biofilm Science Surface Disinfectant Claims UV / UVGI Disinfection Browse all →

Testing services

Gas & VOC

Gas delivery, VOC emissions, device safety panel, gas-phase destruction.

Testing services

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Gas & VOC

Gas delivery, VOC emissions, device safety panel, gas-phase destruction.

Gas Delivery and ControlGenerate, deliver, and verify stable challenge gases with traceable concentration control for device, media, and chamber studies.VOC and By-Product Emissions TestingQuantify VOCs, aldehydes, ozone, and other by-products during device use in controlled chambers.Air Device Emissions Safety PanelRun an integrated chamber panel for ozone, NOx, formaldehyde, and VOCs to support air-device safety decisions.Gas and VOC Destruction TestingMeasure catalytic or oxidative destruction of gas-phase contaminants and quantify removal efficiency and capacity over time.