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Test identification Reference: J001450BS EN 14476:2013+A2:2019Study Title: Quantitative suspension test for evaluation of virucidal activity in the medical area (Phase 2 Step1) Microbiological Solutions
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01
Gather the necessary materials and personal protective equipment (PPE).
02
Ensure that the test method and conditions align with EN 14476 standards.
03
Prepare the test samples according to specified guidelines.
04
Dilute the virus or microorganism to the required concentration for testing.
05
Inoculate the test items with the diluted virus or microorganism.
06
Apply the disinfectant or product under test according to the specified application method.
07
After the designated contact time, neutralize the test samples.
08
Perform appropriate microbiological assays to determine the virus viability.
09
Calculate the reduction in viral load to obtain quantitative results.
10
Document all findings and results in accordance with EN 14476 reporting standards.

Who needs en 14476 - quantitative?

01
Disinfectant manufacturers seeking to validate the effectiveness of their products.
02
Regulatory bodies that require compliance with hygiene standards.
03
Healthcare facilities aiming to ensure that their disinfectants meet required efficacy levels.
04
Researchers conducting studies related to virology and disinfection protocols.
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EN 14476 - quantitative is a European standard that specifies the quantitative testing methods for determining the virucidal efficacy of chemical disinfectants and antiseptics.
Manufacturers and suppliers of chemical disinfectants and antiseptics are required to file EN 14476 - quantitative to demonstrate the efficacy of their products.
To fill out EN 14476 - quantitative, you must conduct the specified laboratory tests, gather data on the results, and complete the required documentation outlining the methods used and evidence of efficacy.
The purpose of EN 14476 - quantitative is to provide a standardized method for testing the virucidal activity of disinfectants to ensure they are effective against viruses and to protect public health.
Information that must be reported includes the product name, the active ingredients, the concentration used, the test methodology, test results, and any conditions under which the tests were conducted.
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