TIK obtains EU Quality Management System Certificate under the MDR
TIK has obtained the EU Quality Management System Certificate under the Medical Device Regulation (EU) 2017/745 (MDR), issued by SIQ Ljubljana.
The certificate covers manufacturing aspects related to ensuring and maintaining the sterility of the medical devices within its scope. This achievement marks an important milestone for TIK and reflects our commitment to quality and regulatory compliance.
We thank all colleagues whose expertise and dedication contributed to the successful completion of the certification process.
