Virology Testing

Your regulatory submissions demand comprehensive testing services tailored to your specific product claims. Element's complete virucidal testing portfolio supports your entire product development journey from initial screening to final submission. Our industry-leading virologists deliver testing for standard and specialized claims, including virucidal efficacy for direct-contact disinfection, residual protection, treated articles, and more. 

• GLP virucidal efficacy testing for regulatory submissions 

• Residual virucidal efficacy testing for long-lasting claims 

• Treated article virucidal testing (fabrics, surfaces) 

• Disinfectant and sanitizer virucidal testing 

• EN virucidal testing for European regulatory compliance 

• cGMP virology testing for pharmaceutical products 

• Custom protocol development for unique applications 

Your antimicrobial products require different testing approaches based on their formulation and application method. We test liquid disinfectants, aerosol sprays, pre-saturated towelettes, treated fabrics and surfaces, residual/long-lasting antimicrobial products, and pharmaceutical products. Our testing capabilities extend across household, hospital, and veterinary applications, ensuring your product efficacy data meets the specific requirements for your intended market. 

• Hard surface disinfectants (liquids, sprays, wipes) 

• Soft surface antimicrobials (fabric treatments, laundry additives) 

• Long-lasting residual products (coatings, treated surfaces) 

• Copper-containing antimicrobial surfaces 

• Antimicrobial pesticide devices

Your product's unique formulation and application require specialized testing methodologies tailored to its specific characteristics. We offer comprehensive testing approaches including suspension-based methods, hard and soft surface evaluations, residual efficacy with wear simulation, surrogate virus testing, and specialized techniques for pharmaceuticals. Our methods support both standard and custom testing protocols across all major regulatory frameworks. Additionally, we provide specialized methodologies for assessing the degree of homogeneity and distribution of virucidal active ingredients, and testing for viral contamination in cell cultures and cell banks compliant with 21 CFR Part 58. 

• Suspension-based testing (ASTM E1052, BS EN 14476, BS EN 14675) 

• Hard surface testing (ASTM E1053, BS EN 16777) 

• Soft surface testing (fabric, laundry additive) 

• Residual efficacy testing with wear simulation 

• Surrogate virus testing for difficult pathogens 

• Topical skin products using ex-vivo models 

• Disinfection validation/qualification (USP 1072) 

• Custom protocol development for specialized applications 

Regulatory expertise advantage

Your products face complex regulatory hurdles that vary across global markets. Our consultative experts stay current with evolving requirements from major regulatory bodies worldwide, helping you navigate the specific data needs for your product claims. We provide complete regulatory dossier preparation and submission support, and we stand by your side throughout the review process to defend results if questions arise.

• US Environmental Protection Agency (EPA) submission support 
• US Food and Drug Administration (FDA) requirements 

• Health Canada registration guidance 

• Australian Therapeutic Goods Administration (TGA) compliance 

• European Chemicals Agency (ECHA) testing standards 

• Support for both GLP and non-GLP testing requirements 

• Assistance with treated article exemption and related claims 

Element’s Life Sciences network includes dedicated facilities for both antimicrobial and pharmaceutical testing. Element Eagan is recognised as a premier antimicrobial testing laboratory, while Element Concord is known for its expertise in pharmaceutical testing services. Beyond these key sites, our team operates from Life Sciences hubs across the world, providing global access to our expert capabilities. Find your nearest Life Sciences hub on our Locations Page.