QG Medical Devices
QG Medical Devices is a leading manufacturer of Medical Devices in the Middle East. Headquartered in Doha, Qatar, QG Medical Devices boasts a state of the art production facility designed by reputable innovative technology providers from Germany, Switzerland and Italy. QG has proved to be a credible contender in the medical devices industry where progressive healthcare markets of uncompromising standards, such as Europe, started to rely on QG patient-centric products for superior quality. For the same reasons, QG Medical Devices is realizing rapid growth of market share worldwide.
Company details
Find locations served, office locations
- Business Type:
- Manufacturer
- Industry Type:
- Medical Equipment
- Market Focus:
- Globally (various continents)
About Us
What We Do?
QG Medical Devices is striving to become a leading medical devices manufacturer in the healthcare industry worldwide, by continuing to introduce innovative and superior medical devices which guarantee better patient care.
- To introduce cutting edge solutions to the medical devices industry whereby Patient and Medical Staff Care are the core of our innovation
- To provide the international health community with safe, effective, and efficient medical devices of the highest quality.
- To reduce/eliminate (where possible) any potential risks associated with Medical Devices reuse and accidental needle stick injuries.
- Continued R&D and investment to produce innovative medical devices for the benefit of our patients and medical staff, and the community as a whole.
To introduce cutting edge solutions to the medical devices industry whereby Patient and Medical Staff Care are the core of our innovation.
Quality Overview
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.