Maintaining Quality for Life
We recognize that uncompromising Quality and Compliance are vital to our success and the success of our customers. For this reason, many of the world’s leading medical device companies entrust Cirtec on a daily basis with the development of their most critical product technologies.
Our robust corporate Quality Management System drives the high level of documentation, training, supplier management, inspection and validation required to produce the most complex Class III medical devices. Our proven yet flexible Quality system can support or integrate with your own. With Cirtec on your side, you can be confident that your product is being designed and manufactured by a partner with a commitment to Quality at all levels of the organization, and in every Cirtec facility.
In addition to Cirtec’s world class operations, your program will benefit from these other Quality tools, experience, and processes:
- FDA registered and inspected
- ISO 13485: 2003 Certified
- FDA-compliant electronics and software validations
Brooklyn Park, MN
- ISO 13485:2003