CE.way Regulatory Consultants Ltd.
CE.way is a regulatory consulting company based in Europe (Dublin, Ireland and Ljubljana, Slovenia) providing services for medical devices, IVD products and cosmetics. CE.way can act as the European Authorized Representative (EC REP) or EU Responsible person. Our services for medical devices also cover device classification, technical file review, product notifications, GMDN codes, national registrations, labelling review and more. We can help companies from all over the world to achieve EU regulatory compliance and enter the EU market.