We support Market Access registrations for your device or drug within the United States and Globally. 

Looking for an EU Authorized Representative or Person Responsible for Regulatory Compliance?

A European Authorized Representative is defined as being any natural or legal person within the European Union who has accepted a written mandate from a non-EU manufacturer to act on their behalf in relation to specified tasks under MDR or IVDR. We can help assigning your EU Representative or Person Responsible for Regulatory Compliance.