The Medical Device Regulation (MDR) mandates manufacturers to comply with the latest standards when introducing new medical devices to the market. Our global team of experts can help you understand testing requirements for medical products at all stages of their life cycle, including innovative devices and those undergoing material or design changes. We have a newly established laboratory in New Brighton, MN, which is ISO 17025 accredited and follows Good Laboratory Practices (GLP). Our laboratory offers testing services for MRI Safety, Biological Safety, chemistry, packaging, reusable devices, and routine microbiology for medical devices. TÜV SÜD can provide testing support throughout various stages of development.