Synkotech Biocompatible Materials S.L

Verify that the products and the manufacturing process meet the requirements of the applicable regulations. Manage the surveillance system. Being an interlocutor with the health authorities and collaborating with them in the execution of the measures that proceed, such as the withdrawal of the product from the market. Facilitate to the health authorities, the documentation that guarantees the conformity of the products with the provisions of the legislation. Release of the medical device.

Coordinate and supervise the preparation of the technical documentation required for the implementation and proper functioning of the quality management system