With over 30 years of combined experience, GrowthImports is dedicated to ensure the facilitation of a compliant and smooth MDR/IVDR compliant importing process in the European market.
Our goal is to facillitate a smooth importing process in Europe. We will reduce your efforts, minimize risks, maintain flexibility and secure MDR/IVDR compliance while increasing your quality standards.
By designating GrowthImports as your dedicated independent import partner, you can avoid risks, market complications and channel conflicts among your supply chain..
one independent importer for your European importing, financial and registration needs.
Our Solutions
Independent regulatory compliant (MDR/IVDR/MHRA) importing services for worldwide medical companies in Europe and the United Kingdom.
Outsourced PRRC services for micro and small medical companies in Europe and North America to comply with Article 15 (MDR/IVDR)
Dedicated fiscal representative services to help medical companies own a VAT number, smoothly Import goods, reclaim VAT and comply with the European TAX and VAT guidelines.
Drive higher global revenue and better profit margins - increase your speed to market time and penetrate existing and new healthcare markets.
Our expert consultants are ready to explore your international growth opportunities!
Visit our resource section for the latest news, white papers and blogs about the global medical device industry
If you are a non-EU manufacturer, you must comply with the Medical Device Regulation (MDR). The Regulation states that manufacturers must select an importer to
The instructions for use (IFU) pertaining to medical devices substantially differ between the Medical Device Regulation (MDR) and the Medical Devices Directive (MDD). Despite the
The CE Mark is mandatory for medical devices Imported to Europe. Learn how your products can get CE marking based on Medical Device Regulations. When
If you are a non-EU manufacturer, you must comply with the Medical Device Regulation (MDR). The Regulation states that manufacturers must select an importer to
The instructions for use (IFU) pertaining to medical devices substantially differ between the Medical Device Regulation (MDR) and the Medical Devices Directive (MDD). Despite the
The CE Mark is mandatory for medical devices Imported to Europe. Learn how your products can get CE marking based on Medical Device Regulations. When
