Established in 1994 with over 30 years of expertise, MDSS is a leading Authorized Representative for In Vitro Diagnostics and Medical Devices, specializing in Regulatory Affairs. Certified to EN ISO 13485, we serve as the main contact for EU Competent Authorities, MHRA, Swissmedic, FDA and TGA. Our services, among others, include EU and Swiss Representation, UK Responsible Person, U.S. Agent and Australia Sponsor, ensuring your company's forefront position in regulatory compliance.