Compliance with DIN EN ISO 13485 for manufacturers of medical devices
Ensure the quality of your medical devices by establishing a quality management system (QMS) with Valicare.
The QMS described by ISO 13485 is tailored to medical devices. It is similar to the requirements of ISO 9001 but significantly more extensive in terms of overall effort and implementation.
Special features must be observed when setting up a quality management system in accordance with ISO 13485 and mapped in the quality management manual. This includes the design documents and the development file for the respective medical device, as well as the verification and validation of the described design.