Iuvo BioScience performs routine on-site testing for the evaluation of viable and nonviable contamination in cleanrooms.
Cleanroom Validation, Maintenance, and Risk Assessment
Our trained staff offers consultation regarding cleanroom validation, maintenance, and risk assessment to ensure compliance to current standards as specified in ISO 14464-1, ISO 14464-2, USP <1116>, USP <797> and USP <800>. Our services include supplying the appropriate growth mediums (contact and fallout plates), incubation and enumeration of samples, as well as performing testing and providing detailed reports. The sponsor may request samples for speciation or gram stain.
Contact Us Today
If you’re seeking comprehensive medical device services, look no further than iuvo Bioscience. Our experienced team is ready to assist you with testing, evaluation, and regulatory support to ensure successful commercialization of your medical device. Contact us today to discuss your project and learn how our expertise can help you get to market fast.