1. About Analytice: A Professional Third-Party Testing Service in France
Analytice is a professional testing service provider established in France in 2001, certified under the ISO 9001 international quality management system. While Analytice does not operate its own laboratories, it partners with an extensive network of specialized laboratories across sectors such as chemistry, materials, cosmetics, pharmaceuticals, food, biology, toxicology, and environmental sciences.
Its primary role is to assist businesses and research organizations in submitting samples to the appropriate testing laboratories, providing tailor-made solutions, expert consultation, and rapid support. It is a trusted testing partner for numerous premium European brands.Through Analytice's coordinated testing protocols and analytical reports, the data generated is both scientifically valid and internationally credible.
2. What Is Vaccinia Virus, and Why Is It a Benchmark for Disinfection Testing?
Vaccinia virus is a member of the Poxviridae family. It is a large, enveloped, double-stranded DNA virus, structurally complex and genetically related to the smallpox virus. Historically, it was used in smallpox vaccines to prevent infection.
Although it is no longer used as a vaccine, the virus is considered low-pathogenic—an infection may only cause mild skin reactions such as rashes, pustules, and slight fever, usually resolving within a few weeks.
Because of this mild pathogenicity and its similarity to more dangerous enveloped viruses like H1N1 or coronaviruses, Vaccinia virus is widely used as a standard model in antiviral efficacy tests.
Under European antiviral testing standards such( as EN 14476+A2:07-2019), any product proven to effectively kill Vaccinia virus is also considered likely effective against other enveloped viruses.
3. Highlights from Our Product’s Antiviral Test Results
We submitted our product for antiviral testing through Analytice, following the EN 14476+A2:07-2019 standard protocol. The testing simulates real-world conditions by using relevant concentrations and contact times to evaluate efficacy against Vaccinia virus.
✔Test Results:
The laboratory report confirms that our product achieved a 99.99% kill rate of Vaccinia virus under both clean and dirty conditions, meeting the threshold for antiviral product classification.
- Clean Conditions:
Represents pre-cleaned environments or surfaces. Under these conditions, the product eliminated 99.99% of the virus within just 30 seconds.
- Dirty Conditions:
Represents contaminated or uncleaned environments. Under these harsher conditions, the product achieved 99.99% elimination within 30 minutes.
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4. Why Do We Insist on International Testing?
✔Testing conducted by internationally accredited laboratories enhances brand credibility and professionalism.
✔Complying with EU antiviral product standards ensures greater consumer safety and peace of mind.
Through internationally recognized third-party testing, we can confidently communicate the efficacy and reliability of our products—letting scientific data speak on our behalf. This is how we demonstrate our commitment to product quality and consumer health.We Believe That True Product Value Lies in Standing Up to Scientific Scrutiny
We will continue to work with international testing bodies, invest in research and development, and build a line of trustworthy, functional cleaning and protective solutions you can rely on—now and in the future.