Medical Device Training from RAPS


The GMDN Agency is promoting best practice in medical device regulation with RAPS. Join the Regulatory Affairs Professionals Society (RAPS) and industry experts at the following event:
• 510k and working with the US FDA, Dublin 24/25 April: https://www.raps.org/events-training/510(k)
• EU MDR/IVDR workshop on real world implementation experience, Brussels 16/17 May: https://www.raps.org/events/transitioning-to-the-new-eu-mdr-and-ivdr-a-workshop-on-real-world-implementation-experiences