Our virology testing capabilities for medical devices cover a range of testing requirements, including testing for the virucidal efficacy of antimicrobial finishes used on the device and disinfectants used during the manufacturing process.
Our experienced scientists and state-of-the-art facilities utilize the latest methods and technologies to provide accurate and reliable results. We offer a variety of testing methods, including suspension testing, carrier testing, and in vitro testing, to meet the specific needs of each device.
We stay up-to-date with the latest regulatory requirements and industry standards, including ISO 21702:2019, ASTM E1053-20, and EN 14476:2013+A2:2019. This ensures that our testing meets all necessary guidelines and can be used to support regulatory submissions.
For tissue product medical devices, viral clearance testing is crucial to ensure that the product is free from infectious agents that could cause harm to patients. At Nelson Labs, we offer viral clearance testing for tissue products, including skin grafts, bone grafts, and other tissue-based implants. Our viral clearance testing services use the most advanced techniques to assess the efficacy of the manufacturing process in removing or inactivating viruses and other infectious agents.
Our experienced scientists will work with you to develop a customized testing plan that meets your specific needs and regulatory requirements. We can provide support throughout the entire process, from study design and sample preparation to final data analysis and reporting.
