KiOmed Pharma SA

• Federaal Agentschap voor Geneesmiddelen en Gezondheidsproducten/ Afdeling Gezondheidsproducten
  BelgiqueContacter l’autorité →

Dispositifs placés dans 3 pays

• Espagne1
• Italie1
• Pologne1

6 contacts identifiés

• DA
  DESCHAMPS Audrey

  PCVRR
  Voir le profil →
• LK
  LENDERS Kevin

  PCVRR
  Voir le profil →
• TE
  THÉATRE Emilie

  PCVRR
  Voir le profil →
• THÉATRE Emilie
  Ensuring that the conformity of the devices is appropriately checked, in accordance with the quality management system under which the devices are manufactured, before a device is released.
  Masqué
• DESCHAMPS Audrey
  - Ensuring that the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date. - Ensuring that in the case of investigational devices, the statement referred to in Section 4.1 of Chapter II of Annex XV is issued.
  Masqué
• LENDERS Kevin
  - Ensuring that the post-market surveillance obligations are complied with in accordance with Article 10(10). - Ensuring that the reporting obligations referred to in Articles 87 to 91 are fulfilled.
  Masqué

• KiOmed — BE-MF-000012034
• KiOmed — BE-PR-000057171
• DEKRA Certification B.V. — 2 certificats — KiOmed
• DESCHAMPS Audrey — KiOmed
• LENDERS Kevin — KiOmed
• THÉATRE Emilie — KiOmed