FDA Issues Guidance on Submissions to Device Identifier Database The Food and Drug Administration has released guidance to manufacturers for submissions to its Global Unique Device Identification Database (GUDID). Read more here. By admin|2014-06-11T16:02:31+00:00June 11th, 2014|Business, Regulatory|Comments Off on FDA Issues Guidance on Submissions to Device Identifier Database Share This Story, Choose Your Platform! FacebookXLinkedInEmail Related Posts OEM trade groups may be seeking to expand definition of ‘remanufacturing’ quickly and quietly Gallery OEM trade groups may be seeking to expand definition of ‘remanufacturing’ quickly and quietly March 24th, 2022 Considerations for effective healthcare vendor management in 2022 Gallery Considerations for effective healthcare vendor management in 2022 December 9th, 2021 Copyright Ruling May Pave Way for Greater Access to Medical Device Service Manuals Gallery Copyright Ruling May Pave Way for Greater Access to Medical Device Service Manuals November 2nd, 2021 FDA Says Sharing Device Manuals With ISOs Does Not Create Cybersecurity Concerns Gallery FDA Says Sharing Device Manuals With ISOs Does Not Create Cybersecurity Concerns September 7th, 2021 FDA Remanufacturing Guidance Comment Period Extended Gallery FDA Remanufacturing Guidance Comment Period Extended August 5th, 2021
