Objective achieved! A few months ago we told you about obtaining the ISO 13485 Quality Management System certification for the Manufacture of Medical Devices in the IKOR plant in Spain.
Now, we are proud to tell you that we have obtained certification for our plant in Mexico.
The electro-medical sector is well known for its stringent requirements and at IKOR we are aware of this and work continuously to ensure that we maintain this level. ISO 13485* certifies the high reliability and technical standard of the solutions developed by IKOR Mexico for the medical sector.
As with the previous certification process, it has required the effort of the whole team to adapt the processes of design, development and manufacture, as well as the introduction of the exhaustive control measures necessary to ensure compliance with the high standards of the medical sector.
We would like to thank and congratulate the entire team responsible for this process for their commitment and effort. We look forward to giving you more equally good news in the near future!
*The UNE-EN ISO 13485 standard specifies the requirements for a quality management system for the design and development, production, installation and servicing of medical devices, and the design, development and provision of related services.
For more information about UNE-EN ISO 13485 click here