Third-Party Verification of AIr Disinfection Efficacy Claims


  • Small non-enveloped RNA strain
  • Aerosolized Pathogen Species
  • Bio-Aerosol Test Chambers
  • Test Room Size 800 Cubic Feet C
  • Contact time 30-60 minutes

KILLS 99.9999% BACTERIA Airborne Surrogate

  • C diff – Clostridioides difficile
  • TB Tuberculosis
  • Enterococcus faecalis
  • Streptococcus Species
  • Pseudomonas aeruginosa
  • Methicillin Resistant Staphylococcus aureus (MRSA)

Kills 99.99% Mold

  • Cladosporium Cladosporioides

Even though air cleaning devices don’t have to be registered, the EPA does have guidelines for the appropriate type and size of bio-aerosol chamber in which to test. Scientific Air Management products are tested under these guidelines and have Laboratory tested kill rate of up to 99.9995% of airborne norovirus surrogate (one of the most difficult viruses to kill) and 99.9999% of bacterial surrogate including TB and C-diff representative pathogens.

Two independent, nationally recognized lab facilities (Environmental Diagnostics Laboratory and MicroChem Laboratory), using these guideline conditions, performed efficacy testing of airborne pathogen. The following are the tests results and compiled reports.

Per suggested guidelines, Scientific Air Management adhered to the following test protocols:

Test methods employed

Contact time (minutes vs. hours)

Type of pathogen

Killing percentage (minimum 99.9%)

Air Disinfection Field Studies

The conditions above are difficult to apply in field studies and are hard to accomplish in hospital settings.


For field studies to achieve the same efficiency in testing parameters, they should be conducted at unbiased facilities with the same scientific test conditions that eliminate all testing room variables, like:

Variable source contamination

Personnel and visitor traffic

Equipment movement

Open doors

HVAC inefficiencies

Concise testing should only include the pathogens being tested and the air management device itself within a standard size room.

The field study below, Pharmacy Compounding, is the closest on-site testing to match laboratory conditions. Due to the nature of the sealed and closely regulated pharmacy Anteroom and ChemoRoom, laboratory-like conditions were achieved as the tests were performed in these areas.