After several months of joint work between those responsible for the Quality and Regulatory area of Mechanized Gabriel S.A. and specialists of KEYMED Devices in the comprehensive review and fine-tuning of their Quality Management and Good Manufacturing Practices system and the revision of the Historical Design Registers of their products in accordance with the requirements of ANMAT Provision 3266/13, the January 23 and 24 have been audited by ANMAT inspectors successfully approving it and proceeding with the renewal of its current rating as a manufacturer of medical products.