Qatari German Company for Medical Devices (QGMD) is certified for EN/ISO 13485:2016;Quality Management System Standard Required for Medical Devices, ISO 9001:2015; the generic Quality Management System Standards.

QGMD manufactures medical devices according to established Quality Management System.All the documentations, processes, procedures, instructions and the records are reviewed by the certifying body during the audit process to assess the adequacy and compliance. These certifications are subjected to periodic checks and under the close monitoring of the certifying body. In addition, a trained team of internal auditors are periodically reviewing the functions of the Manufacturing, Quality Control, Material & Resource Management and Training processes. QGMD maintains and control system documentation and records including those of product and process conformity as required by the management system standard.

All of QGMD products are certified for CE Mark in compliance to European Medical Device Directive MDD/93/42/EEC including its amendments.

QGMD perform all of its operations in compliance with GMP rules.

QGMD products registered and approved by Health Authorities in various countries and the registrations are maintained and renewed periodically.

Q Safe - Re-use Prevention Syringe - Brochure

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