We use cookies to provide you with a better experience. By continuing to browse the site you are agreeing to our use of cookies in accordance with our Cookie Policy.
Accept
Home » UDI Documentation for Class III Devices Should Be Ready: Expert
UDI Documentation for Class III Devices Should Be Ready: Expert
With investigators from the U.S. Food and Drug Administration set to begin scrutinizing UDI compliance, Class III devicemakers should ensure that UDI changes in their design history files are adequately documented and that a verification process for barcodes is in place.
To View This Article:
Login
Subscribe To International Medical Device Regulatory Monitor