As a partner of advanced manufacturing in the medical device arena, the ISO 13485:2016 certification represents our commitment to producing high quality electronic medical manufacturing services.

Veris takes our commitment of providing the highest quality advanced manufacturing very seriously. In order to upkeep our high standards, we have a skilled five person team of ISO13485 internal auditors certified to conduct monthly internal audits. They search for areas of improvement as well as areas of continued excellence. External surveillance audits are then performed once a year and re-certification audits performed every three years. In order to become and remain certified, we must conduct regular audits to ensure an outstanding and effective quality system is established and maintained through a compliant Quality Management Systems (QMS).

During the last week of January 2020, Veris was audited by ABS Quality Evaluations, who found no major non-conformances.