Usually, people have their biocidal product tested against a virology standard to make a claim against either a certain virus or a generalised antiviral claim. The product type will determine which virology standard is most relevant, or for specialist products we can write bespoke methods. The product type may also limit the number of claims that can be made. One example of this is that with hand sanitisers, you can make antiviral claims with the correct test, but you may not be able to make specific claims against diseases as well, if classing the product as a biocide. Making claims against specific diseases that are meant for human disinfection can push the product into medical device territory rather than a biocidal, meaning that the product will fall under different regulations. For more information about making specific claims on hand sanitisers you can contact the MHRA who are the governing body for medical products.
For disinfectants that aren’t intended to be used on humans, more specific claims can usually be used. According to the ECHA, if you have efficacy data against a specific organism and the testing was realistic to how the product shall be used, then you can make a claim. Although the ECHA does state this is generally looked at on a case-by-case basis, so it may be worth speaking to the HSE first (they are the responsible for biocidal regulations in the UK). We have a large library of organisms, and you can find out more about these on our organism fact sheets page. We can also purchase additional organisms for specific projects.
Virucidal testing
Virucidal testing is very different from other anti-microbial testing, and this is because of a couple of reasons. One of them being that the viruses are ‘grown up’ on living cells rather than on the usual agar/culture media we use for other types of organisms. This can cause problems if the product has a cytotoxic effect. A cytotoxic effect is when the product itself damages or kills the cells. When this happens, it isn’t possible to tell whether the test criteria were met, and the test would be invalid. At Melbec, we have put two different processes in place to reduce the cytotoxicity of products. These methods are LVP and micro spin plating. As far as we know, we are the only lab in Europe that doesn’t charge extra for this service and is included in our already competitive prices!
To determine whether the test will be a pass, we count the number of cells that are left alive. The more cells that are alive, the less virus there is. If there are fewer cells left, it shows that less of the virus has been killed. This is because viruses live off and destroy the cells in the process. If the product is cytotoxic and has killed the cells, we have no way of telling whether there is any virus left or not.
Standards
Below are the products that we commonly test and the standards that are required for each. You can click on the standards to find out more about them.
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