Quality Assurance & Regulatory Affairs

The Quality Assurance & Regulatory Affairs team at Viant Medical is responsible for ensuring that all medical devices and technologies meet stringent quality standards and regulatory requirements. This team works to maintain compliance with global regulatory bodies, conduct quality audits, manage risk assessment, and ensure product safety and efficacy from design through to manufacturing and distribution. Their efforts are crucial in guaranteeing that Viant's products reliably serve healthcare providers and patients worldwide.