EU MDR Extension: Don’t Make Medical Device Product Labeling an Afterthought

Recognizing the critical need to mitigate the risk of medical device shortages and recalls for patient safety, the European Parliament recently granted an extension for EU MDR compliance. Watch this webinar and learn how to ensure compliance and mitigate risk of recalls.

EU MDR Extension: Don’t Make Medical Device Product Labeling an Afterthought is a webinar from Loftware focused on Data. See Loftware's website for confirmed availability and schedule details. UPCOMING provides an independent event listing and directs attendees to Loftware's website to complete registration or viewing.