We are proud to announce that after an external audit, the Quality Management System of C&J Industries, Inc. has been assessed and approved by DQS, Inc., and fulfills the requirements of the ISO 13485:2016 and ISO 9001:2015 standards.
These re-certifications, completed December 2023, each consist of a complete certification audit every 3 years with yearly surveillance audits, to verify that the C&J Industries’ Quality Management System continues to meet the requirements for ISO 13485 and ISO 9001.
Since 2009, C&J Industries has partnered with DQS, an accredited certification body, to achieve these ISO certifications.
“These certifications reflect our long-standing commitment to maintain high levels of quality and reliability to meet or exceed our customers’ expectations,” said Cameron Costner, Regulatory Affairs Administrator at C&J Industries. “We will continue to look for opportunities to improve our processes and ensure our Quality Management System remains effective.”
ISO 13485 is the globally recognized standard for organizations involved in the design, production, installation and servicing of medical devices and related services.
ISO 9001 is a globally recognized standard for quality management. It helps organizations of all sizes and sectors to improve their performance, meet customer expectations and demonstrate their commitment to quality.
Learn more about our quality policies and view our certificates here.