Corvalent Passes 2016 ISO Certification - Excelling in Quality Management Another Year
Corvalent passes ISO certification on their surveillance audits this year for ISO9000-2008 and ISO13485-2003.
Each year, we continue to make every necessary change to stay on the leading edge of quality and performance. Our ISO certification is only a standard. To us, exceeding expectations means delivering high quality products and services built for longevity, enabling our customers to make the most of their application.
ISO9000-2008 is a set of quality control international standards an organization has to meet to qualify for certification of their products or services.
ISO13485-2003 is an international standard that defines the requirements for a comprehensive management system for the design and manufacture of medical devices.
“It is very rewarding to achieve ISO13485:2003 certification. Our continuing success passing surveillance audits without any corrective actions just confirms the well-designed and implemented Quality System at Corvalent” - Ana Rudloff, Quality Assurance & Document Control Specialist.
She adds, “Our entire team has become self-aware and motivated to the highest quality standards. It is an effort we are all very proud of. Striving and pushing ourselves to achieve the highest levels of operational excellence in serving our customers.”
With new efficient processes beginning in January of next year, Corvalent plans to upgrade both ISO standards by September 2017.