Quality is the basis of our success.
Quality is a central safety parameter in medical technology, as here the focus is on people's health and quality of life.
Highly qualified employees and consistent development of the quality management system in order to fulfil completely the constantly growing requirements of the medical devices industry not just today, but also in future, are the guarantors of Josef Ganter Feinmechanik’s quality claim. In doing so, we place great importance on transparent processes and professional processing of assignments.
Due to the amendment to the EU medical devices regulation (MDR), the workload of all OEM manufacturers for the development and production of medical implants and components will be increased significantly in future and thus also the requirements regarding certification and auditing. As a manufacturer of medical devices and as a contract manufacturer (according to customer specification) with our own regulatory affairs management, we can build on years of experience in OEM/PLM setups and know how to design contracts for comprehensive resource management and for the required assuring of traceability.
We would like your workload in the development, manufacture and approval of your medical devices to remain manageable.