PRO MD SERVICE

It is a long way from the idea of your product to market readiness. We support you along the way in implementing the legal requirements for the market approval of your medical devices. We are experts in this and are at your side as a partner for solving your requirements. We open doors... With our service we offer you the assumption of the EU authorized representative (EU-Rep) with all associated obligations or parts thereof... For medical devices and IVD, services such as EU-Rep, Technical File, QMS Quality Management System, Audit, Inspection, CE, Registration, MDR, IVDR, Supplier Management, CSV Computer System Validation, Person Article 15, QMB Officer, EU, Compliance.