What is your quality record?
TriVirix has a 99.6% customer acceptance rate, and our facilities are routinely audited by the FDA.

How does TriVirix ensure consistent quality?
TriVirix specializes in Operational Excellence – the delivery of category-leading manufacturing and supply chain performance through customer focused improvement and execution. TriVirix’s global state of the art manufacturing facilities are ISO 9001/ 13485 certified, FDA registered and QSR compliant, ensuring that we consistently provide exceptional quality and service, on-time and on budget.

How can TriVirix help me meet stringent government regulations?
Since TriVirix is 100% dedicated to manufacturing medical and life science equipment, we understand the challenges that are unique to medical and life science manufacturing. We know that customers must comply with stringent government regulations (such as the FDA's QSR) and are prepared to help them navigate through the complex compliance issues. This includes helping them maintain detailed policies, protocols and procedures that ensure the integrity of the product manufacturing and distribution processes. Our pre-production quality planning process ensures that your products will be free from defects in workmanship of material, and will always comply with regulatory agency approval.

Has TriVirix ever been audited by the FDA?
TriVirix’s facilities are routinely audit by the FDA either as part of their audit process or during the transition of a new customer product into one of our facilities.