Quality is critical to our business because lives depend on us.
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 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.
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. All Viant employees are committed to developing and continuously improving products and processes through measured quality objectives.
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