LOUISVILLE, Colo.--(BUSINESS WIRE)--One day before the U.S. Food and Drug Administration’s (FDA) deadline for medical device companies to submit Class III product data to the FDA’s Production Global UDI Database (GUDID), GHX announced that in August its UDI solution and services practice successfully submitted UDI data attributes in the required Health Level 7 Structured Product Label (HL7 SPL) format to the GUDID. GHX Business Consulting Services has been helping numerous medical device manufacturers prepare for UDI for many years, and its UDI technology solution was able to submit data for Class III devices for one of the industry’s largest medical device companies well in advance of tomorrow’s deadline.
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