Market Access Consulting
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.