Sanrubio supports Medical Device companies throughout the registration process before regulatory health authorities in the United States (FDA), Argentina (ANMAT) and Brazil (ANVISA) and provides specialized regulatory consulting services for regulatory compliance related to Medical Devices: ISO 13485, MDSAP, Regulation 21 CFR 820, Good Manufacturing Practices, etc. In a business where quality and safety come first, we have the necessary tools to overcome any challenge. Our multidisciplinary approach allows us to create methodologies and strategies aimed at generating value and trust.