STEMart, a US-based provider of comprehensive services for all phases of medical device development, is pleased to announce that it offers Disinfection Validation Services for reusable medical devices. These services are designed to ensure that products meet FDA requirements for disinfection validation and patient safety.
STEMart has recently introduced Bioburden Tissue Testing services for medical applications, including Aerobic Count, Anaerobic Count, Fungi/Mold Count, and Spore Count.
STEMart has recently introduced Microbial Identification and Strain Typing services with unmatched accuracy from the most relevant bacterial, filamentous fungi, and yeast reference libraries.
STEMart introduced the Biological Indicator-Population Verification testing service that can be applied to all types of biological indicator configurations.
STEMart introduces multiple medical device genetic toxicology testing services following the OECD guidelines modified for medical devices and performing under GLP conditions.
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