Webcast overview
COVID-19, social distancing measures and the obligation felt by the Medical Device industry to prioritize response efforts and reduce any production shortages of necessary supplies to battle this global pandemic, has resulted in the European Parliament voting to delay the implementation of the EU MDR regulation. The European Parliament has officially provided Medical Device Organizations a 12-month reprieve on the European Medical Device Regulation (EU MDR) thus allowing companies the ability and most importantly time in getting their houses in order.
In this webcast, Vishal Pathak, Life Sciences Advisory Manager, Richard Castle, Global Sales Manager Medical Devices at PRISYM ID and Kevin Grygiel, VP Strategic Accounts & Partner Ecosystem at PRISYM ID will delve deeper into the impact of changed EU-MDR timelines and key insights into how the medical device industry will meet labeling and packaging compliance from a Global perspective.
Featured speakers
