Quality Culture

The people behind Viant understand that we’re not just manufacturing products—we’re making components and finished devices that will be used to save or enhance a patient’s life. Our Global Quality Vision and Quality Policy are designed to ensure consistent high quality and compliance at every location, on every project, at every stage of the product lifecycle.

Quality Vision

Quality is at the forefront of everything that we do because lives depend on us. To achieve this vision, we pledge to maintain a medical device manufacturing culture of quality and compliance.

We will strive daily to achieve our mantra: Quality for Life.

Quality Policy

Viant is committed to providing quality medical devices and components that are used to save or enhance the lives of the patients we serve. We will maintain compliance with current quality and regulatory requirements as well as those of our customers.

We will monitor, manage risk and take action throughout our processes to ensure the continued effectiveness of our quality system.

Regulatory and Compliance

With 50+ years of medical device experience, we have developed a thorough understanding of the complex regulatory environment. Every product is manufactured to exact specification, in full compliance with FDA guidelines.

ISO 13485 Certified
FDA Registered and compliant with the Quality System Regulation cGMP
ISO 14971 Risk Management Certified
Class I, II, and III devices, including Premarket Approval (PMA) product support
ISO 7 and ISO 8 Certified Cleanroom Controlled Environments
Metrology laboratories
Bioburden laboratory

Viant Medical services

Design & Development

Design for Device Assembly (DFA)