The transition deadline for the European Medical Devices Regulation (MDR 2017/745) will be here soon and medical device companies are preparing to recertify under the new regulation. However, some manufacturers could face another obstacle: losing their Notified Body (NB).
Some EU Notified Bodies may not continue their operations under the MDR, leaving their clients without a certification partner at this critical time. However, there are steps you can take to prepare for this possibility. In this white paper, we will discuss how to prepare to change your Notified Body. You will learn:
You will learn all this and more in this 9-page white paper.