How prepared is your organization for compliance to the European Medical Devices Regulation (MDR2017/745)? Technical documentation forms the heart and soul of any manufacturing facility and it’s guaranteed to be reviewed in a CE audit. It is important for manufacturers to have a clear understanding of what their progress is with the transition and what needs to be done to maintain market access. Our MDR Readiness Assessment for Technical Documentation is a simple easy to use checklist designed around each and every clause of the new MDR2017/745. It will help you clause by clause, assess what the current state of your technical documentation is and allow you to easily see where your gaps lie.