If your company sells medical device parts into the EU, you may need to acquire data on any products in scope of the EU MDR in order to maintain market access and avoid reputational damage. However, many companies have yet to implement the systems, processes and training needed to meet their requirements. This guide outlines eight steps to an effective EU MDR program, and suggests solutions for companies as they manage their supply chain data and educate suppliers on requirements.
Protect your company from the risks associated with medical device requirements. Download your copy of the guide now.