Disinfectant Efficacy Testing Services
Tip: Click the methods listed in bold for a summary with strengths and weaknesses.
If you are interested in registering a disinfecant product or adding to label claims you may find EPA's disinfectant testing requirements or our list of available microorganisms helpful.
EPA-Accepted Disinfectant and Sanitizer Test Methods (GLP Testing Available)
- AOAC Use-Dilution Test for Disinfectants
- AOAC Germicidal Spray Products Test
- EPA Presaturated Towelette Disinfection & Sanitization Tests (Germicidal Wipes Tests)
- AOAC Germicidal and Detergent Sanitizing Action of Disinfectants Test (Food Contact Sanitizer Test)
- ASTM E1153 Non Food-Contact Sanitizer Test
- ASTM E2197 ("QCT II" Quantitative Carrier Test, for Clostridium difficile)
- AOAC Chlorine Equivalency Sanitizer Test
- AOAC Fungicidal Activity of Disinfectants Test
- Quantitative Time-Kill Test (Liquid Suspension of Bacteria)
- Quantitative Time-Kill Test (Film of Bacteria Dried onto Test Surface)
- Minimum Inhibitory Concentration Test (MIC Test)
- Minimum Bactericidal Concentration (MBC) Test
- Disinfectant Neutralization Testing
- "Real-Life" Disinfectant Efficacy Testing
- Virucidal Efficacy Tests
- Modified AOAC Germicidal Spray Products Test
- Modified Presaturated Towelette Disinfection & Sanitization Tests
- Quantitative Kill-Time Test (film of viruses dried onto test surface)
- Quantitative Kill-Time Test (viruses in liquid suspension)
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Disinfectant and Sanitizer Testing and Screening Methods (Cost-Effective and Quick)
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Virucidal Disinfectant Testing Services (Full Virology Services Available Sept. 2010)
Note: Select bacteriophages (viruses that infect bacteria) are used for the services outlined below - using bacteriophages to gauge the virucidal efficacy of a disinfectant is smart, remarkably fast, and relatively inexpensive!
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Not seeing the test you're after? Try our Complete Test Menu. If that doesn't work, give the laboratory a phone call and we'll see if we can help you out.
Note: "GLP" stands for Good Laboratory Practices, and refers to governmental requirements for laboratories that submit data to EPA or FDA.
