EU MDR
I am text block. Click edit button to change this text. Lorem ipsum dolor sit amet, consectetur adipiscing elit. Ut elit tellus, luctus nec ullamcorper mattis.
Medical devices services with regard to the EU MDR
EU MDR General Requirements
Quality Management System
Technical Documentation
Clinical Evaluation
Clinical Investigation
PMS and PMCF
SSCP
Quality Management System
Interested in our services?
Contact AKRA TEAM for support, hands on implementation services and personalized training by experts with key competencies in the areas listed above.