MDR REGULATOR

MDR Regulator is built by a group of specialists with long-standing experience in legal regulations, medical technologies, lobbying, business management and marketing. We have knowledge concerning all risk classes of medical devices and borderline products, as well as experience in cooperation with notified bodies, competent authorities, accreditation bodies and the European Commission. We are well aware of the process approach to quality assurance according to ISO 13485 and ISO 9001, which is very important in the medical industry. Our activity relies on a highly qualified team, whose members - as part of sustainable development - constantly improve their qualifications, as well as openness to new solutions and development paths... MDR Regulator offers a full range of services enabling medical device manufacturers to place their products on European markets and to ensure continuity and compliance of their operations with applicable European laws... As a team of medical market..

Also known as: MDR Regulator Sp, MDR Regulator sp. z o.o.

VAT numbers: PL5272926228