ISO Certification Announcement
December 19, 2018
Upon completion of an extensive medical device quality management system evaluation, More Diagnostics, Inc. has achieved ISO 13485:2016 certification. This certification includes compliance to MDSAP, Canada MDR, Brazil ANVISA and US FDA 21 CFR 820 requirements. More Diagnostics, Inc. demonstrated its ability to provide medical devices and related services that consistently meet customer and applicable regulatory requirements. The scope of the evaluation includes design and development, manufacture, storage, distribution and post-market surveillance of a medical device.
More Diagnostics, Inc.'s success in achieving ISO 13485:2016 certification is a proactive one. Always aiming at improving our products and services, More Diagnostics, Inc. continues to advance their ISO certification. This result could not have been achieved without co-operation within the company. This success demonstrates our commitment to providing quality products and services to our customers and partners.
We look forward to new opportunities and projects with long-time and new partners and customers.« Back to News