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Standard Test Method for Neutralization of Virucidal Agents in Virucidal Efficacy Evaluations
STANDARD published on 10.10.1998
Designation standards: ASTM E1482-92(1998)
Note: WITHDRAWN
Publication date standards: 10.10.1998
SKU: NS-41914
The number of pages: 2
Approximate weight : 6 g (0.01 lbs)
Country: American technical standard
Category: Technical standards ASTM
Keywords:
Cytotoxicity, Disinfectant, Gel filtration, Inanimate nonporous surfaces, Microbiological examination, Neutralization, Nonporous surfaces, Tissue culture, Virucidal neutralization method, neutralization-virucidal agents in virucidal efficacy evaluations (for, use on inanimate nonporous environmental surfaces), test, ICS Number Code 11.080.20 (Disinfectants and antiseptics), 71.100.35 (Chemicals for industrial and domestic desinfection purposes)
| 1. Scope | ||||
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1.1 This laboratory test method is intended for use in conjunction with evaluations of the virucidal efficacy of disinfectant solutions or pressurized disinfectant spray products intended for use on inanimate nonporous environmental surfaces or for other special applications. The test method may be employed with all viruses and host systems. 1.2 This test method should be performed only by persons trained in microbiology and virology. 1.3 This test method utilizes gel filtration technology. The effectiveness of the test method is dependent on the ratio of gel bed volume to sample size and uniformity in the preparation of columns and centrifugation conditions. The effectiveness of this test method is maximized by investigator practice and experience with gel filtration techniques. 1.4 This test method will reduce, but not necessarily eliminate, disinfectant toxicity while preserving the titer of input virus. 1.5 The values stated in SI units are to be regarded as the standard. 1.6 This standard does not purport to address all of the safety problems, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use. |
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