How to start? Make an appointment.
The exact scope, as well as the duration and cost of certification, will be determined together prior to the process itself at an informal meeting.
We will create an offer tailored to the characteristics of your company based on the data established at the meeting.
Is your quality management system appropriate and effective with an emphasis on the safety and efficacy of medical devices?
Show that you produce safe medical devices. Maintain compliance with regulations by being certified according to ISO 13485.
The certificate proves that the supplier, repairer, manufacturer or retailer of medical products has successfully implemented, documented and maintains and improves the management system.
