VARI operates its systems to ensure full compliance to external regulatory requirements.
VARI development and manufacturing operations and procedures satisfy the conditions of cGMP. 
VARI maintains full traceable records of all inputs and outputs throughout the manufacturing process. 
VARI have implemented and maintains a quality system in compliance with ISO 9001:2008 and ISO 13485:2004.
ISO 13485:2004 specifies requirements for a quality management system where an organisation needs to demonstrate its ability to provide medical devices and related services that consistently meet customer and regulatory requirements.