ON DEMAND WEBINAR
Duration: 1 hour
In recent years the global regulatory requirements have continued to evolve in many areas, with new interests in a particular area of focus – the Unique Device Identification (UDI). Whilst at a strategic level the global regulators are aligned in recognizing the need to enhance the traceability of supply of medical devices to and through the global markets, the operational reality has seen the beginnings of some level of divergence across countries.
Whilst regulations often stipulate UDI as a requirement, the data submissions around UDI requirements vary from country to country. The implementation of such UDI regulations can vary with country specific requirements, data structure definitions and other political & economic factors creating additional commercial considerations that begin to mandate what type of UDI solution/ label is required. In response to all this complexity the instant reaction is “we need a UDI solution” but what exactly is the type of solution that is needed and how should UDI requirements above those stipulated by country health authority regulators be handled? This webinar is designed to walk you through:
Thank you for your interest in the webinar! Check your inbox for an email with instructions on viewing this on-demand presentation.Download Now
Enter the 6 digit code sent to your mobile number
Click on Resend the verification code again