Disinfectant Efficacy Testing
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The essential role of ensuring your disinfectants are not only effective but also compliant with international regulatory standards. Leveraging our global laboratories, with over 6 decades of expertise in microbiology, we deliver customized disinfectant efficacy testing solutions to meet your requirements.
Our Disinfectant Efficacy Testing Services
We offer a full suite of efficacy testing services for disinfectants, including but not limited to:
Quantitative Suspension Testing: Assess the activity of disinfectants against a wide range of microorganisms under standardized conditions.
Surface Testing: Evaluate the effectiveness of disinfectants on various surfaces using methods such as the EN 13697.
Practical Use Testing: Ensure your disinfectants perform under real-world conditions, simulating practical applications in healthcare or industrial environments.
Regulatory Compliance: Ensure your products adhere to standards set by the EU Biocidal Products Regulation (BPR), FDA, or other global regulatory bodies.
Why Efficacy Testing Matters
Effective disinfection is vital for maintaining safety and compliance in critical environments. Whether you’re launching a new disinfectant or verifying an established product, robust testing helps ensure:
Elimination of harmful microorganisms
Prevention of contamination
Compliance with industry and regulatory standards
Protection of public health
Why Choose Cormica for Disinfectant Efficacy Testing?
Expertise Across Global Standards: Our laboratories are fully equipped to perform testing that complies with key standards, including EN 13697, EN 13727, and EN 16615, among others.
Advanced Facilities: With a global network of laboratories, including Wickham Micro, we bring together industry-leading technology and highly experienced microbiologists to deliver reliable and reproducible results.
Comprehensive Support: From study design to final reporting, we provide end-to-end support to ensure your disinfectants are tested to the highest standards and provide the necessary documentation for regulatory submissions.