Providing safe and effective medical devices that provide customers with a better quality of life is what motivates us to evolve more and more in our manufacturing processes and the development of new technologies.
In addition to the concept of continuous evolution, we have developed the Integrated Quality System, which governs from the acquisition of imported high quality raw material to manufacturing, such as the rigorous method of inspections and tests on quality control and the storage of medical devices.
Our industrial complex was designed to meet the regulatory requirements established in RDC 16: 2013, EN ISO 13485: 2012 and 510K (FDA regulatory standard).
Being part of our organizational culture and pride, all our employees are constantly trained to raise personal development, improve technical skills in the operational processes, habits and attitudes that result in the quality of services provided to our customers.
Osteomed has an integrated quality system that is structured and organized to manage and guarantee the quality, required resources, operational procedures and responsibilities of each employee in the manufacture of medical devices.
“Osteomed is commited to complying with Regulatory Requirement and the effectiveness of its Quality Management System, ensuring Customer satisfaction through the supply of quality products, manufactured in processes continuosly improved”.
GOALS OF THE QUALITY SYSTEM :
- Complying with Regulatory Requirement;
- Effectiveness of the Quality Management System;
- Customed Satisfaction;
- Quality Products;
- Continuous Improvement;
“To exceed the expectations of our Clients, through excellence in the service and supply of medical devices for spine with high quality.”
“To be a leading company in the market, acting with responsibility and excellence in the area of medical devices, recognized by our customers, suppliers, service providers and employees as a benchmark in quality standards.”
Commitment, Professionalism, Ethics and Team Work.