Officers and regulatory representatives of BioCytex
TIDAFI Floriane
1 - Verify of conformity of the devices in accordance with the quality management system
2 - Draw-up and and keep up-to-date the technical documentation and EU declarations of conformity
3 - Ensure the post-market surveillance
4 - Fulfill the reporting obligations referred to in Articles 82 to 86
5 - Ensure that the declarations referred to in Annex XIV, section 4.1, are issued.