With the COVID-19 crisis, the Medical Device Regulations (MDR) have been pushed back one year, this delay has given a respite for those companies that were not quite ready for the increase regulations.
In this session, we will be discussing the current status of the medical device industry regarding MDR and what are others doing to get ready.
Attendees will learn: - What additional requirements are in the MDR? - Where is the industry currently at and how many companies feel ready for their first submission? - What have we learned from the first submissions under MDR? - What are others doing now, to save time and money?
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