Viora is committed to adherence to the highest industry standards in the manufacturing of medical devices. All the products are in compliance with the company’s quality assurance system and are manufactured under ISO 13485. The products also comply with the United States Quality Systems Regulations and GMP standards as well as the requirements of the EU Medical Devices Directive.

Specific systems are also certified with required clearance and/or directives according to the countries where the systems are in use (i.e. U.S. FDA).