Amman Pharmaceutical Industries

No certificates registered for this manufacturer.

4 contacts identified

• AM
  ABUZNAID Maha

  PRRC
  View profile →
• AT
  ADAMAH Tasneem

  PRRC
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• 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.
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• 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 .
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• Federaal Agentschap voor Geneesmiddelen en Gezondheidsproducten/ Afdeling Gezondheidsproducten
  BelgiumContact the authority →

Devices placed in 2 countries

• Belgium1
• Spain1

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