Medtech Manufacturers have been given an additional year to prepare for new European Union regulations, but pivots in business and an altered timeline for Medical Device Regulation may drive the need to comply sooner. How do you refocus and start working towards the transition in the midst of a pandemic? Nicolle Cannon, founder/CEO of Cannon Quality Group, discusses four steps you can employ to move your organization towards compliance now. Whether your interest is in your technical file, risk management, UDI or EUDAMED, this session is recommended for any manufacturers impacted by new EU MDR/IVDR regulations.