Theresa Jeary three-part interview

The medical regulatory landscape is undergoing its most significant overhaul in years. The new EU Medical Device Regulation (MDR) and In Vitro Diagnostic Device Regulation (IVDR) had been four years in the making, and were published in May 2017.

During an in-depth interview, Theresa Jeary, LRQA Medical Devices Technical Manager, shares her thoughts on how the medical device industry will witness a transformation, and advises how manufacturers can take action to prepare for the changes.

This interview is the first of a three-part series on the new regulations, and how the changing regulatory landscape impacts manufacturers and Notified Bodies.