TREVOR, WI, December 16, 2020 – Vonco Products LLC, an industry-leader in the contract manufacturing of liquid-tight medical devices and fluid bags, biohazard transport bags, and infection prevention PPE and equipment covers announced today that the company received certification of their Quality Management System to the requirements of ISO 13485:2016.
“The ISO 13485:2016 certification is great news for Vonco,” said Christie Marr, quality manager at Vonco. “It demonstrates that we have a sustainable quality management system. The certified processes and procedures that we have implemented throughout the facility will help us prove our commitment to quality to our customers.”
ISO 13485:2016 is an internationally recognized quality standard intended to provide a quality framework focused on the consistent design, development, servicing, and sale of medical devices that are safe and effective for their intended purposes. To be certified, organizations must demonstrate an ability to provide medical devices and related services that consistently meet customer expectations and regulatory requirements.
“This certification represents an important milestone for Vonco and reflects our commitment to quality in providing best-in-class contract manufacturing services for our clients,” said Keith Smith, president of Vonco. “We are very proud of this certification as it reflects our rigorous and risk-based approach to design, development and manufacture of liquid-tight medical fluid bags and components for custom medical device applications.”
Vonco (www.vonco.com) is a contract manufacturer of liquid-tight medical device and consumer stand up pouches. We provide fast custom design for the ‘craziest’ of bags with unique shapes, fitment insertions and assembly of unsupported or laminated films. With more than 60 years of experience, we have the flexibility to design and develop your bags in a fraction of the time to increase speed-to-market, lower costs and improve returns on investment.