Amman Pharmaceutical Industries

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

Aucun certificat enregistré pour ce fabricant.

Dispositifs placés dans 2 pays

• Belgique1
• Espagne1

4 contacts identifiés

• AM
  ABUZNAID Maha

  PCVRR
  Voir le profil →
• AT
  ADAMAH Tasneem

  PCVRR
  Voir le profil →
• ADAMAH Tasneem
  Technical documentations has been drawn up and kept up-to-date, sign the EU Declaration of conformity.Ensure and approve the PMS activities are implemented, compiled with EU MDR 2017/745.Ensure that the reporting obligations for incidents and FSCA are fulfilled and comply with EU MDR 2017/745.Review GSPR and CER report and make sure they are complies with EU MDR 2017/745.The primary contact personae with economic operator, notified bodies and complement authority.
  Masqué
• ABUZNAID Maha
  Devices release accordaning with QMS documentation. Ensure QMS covers all parts and elements of a manufacturer’s organization and in complying with EU MDR 2017/745, this includes and is not limited to:Instruction of particular staff whose job includes the release of devices.Internal audits of release procedures and batch history/ release documentation.Periodic sampling of batch release documentation .
  Masqué

• Easy Medical Device — représente — API
• ABUZNAID Maha — API
• ADAMAH Tasneem — API