Dirigeants et représentants réglementaires de VEAG
EGLY Collin
according to Article 15 paragraph 3 MDR:
- the conformity of each devices is appropriately checked prior to their release, in accordance with the QMS under which the device is manufactured
- the technical documentation and the EU declaration of conformity are drawn up and kept up to date
- the post-market surveillance obligations are complied
- the reporting obligations are fulfilled
- in case of investigational devices, a statement is issued