INTRA-MED Spółka z ograniczoną odpowiedzialnością

Adequate verification of the conformity of products in accordance with the quality management system in which these products are manufactured, before the release of the product; Preparation and ongoing updating of technical documentation and EU declaration of conformity; Compliance with post-market surveillance obligations in accordance with Article 10(10) of the MDR; Compliance with the notification obligations referred to in Articles 87-91 of the MDR