SERIOUS ABOUT QUALITY

BIOVIC’s commitment to improving the quality of life for our patients guides every aspect of our operations. We take the responsibility of manufacturing and delivering quality vascular graft products very seriously. This is reflected in the facilities we use.

BIOVIC's 4000 square foot state of the art facility at Sunway Damansara Technology Park houses a Class 10,000 clean room, fully equipped Research and Development and Quality Control labs, offices, and conference room. A complete manufacturing line for the production of PTFE Vascular Grafts has been developed, commissioned, and is now fully operational.

BIOVIC is ISO 13485 (2016) certified and its products are approved by the European Union (CE Mark, MDR Certification Date : June 21 2024) and the Medical Devices Authority (Malaysia). United States FDA clearance is now in process.