There’s a mounting list of regulations aimed towards Unique Device Identification (UDI), intended to improve patient safety, supply chain efficiency and post-market surveillance. The benefits are numerous, but challenges continue for medical device suppliers on their long – and often painful – journey to tackle those UDI requirements. And confusion remains as we often hear the question, “Are PIM and PLM equally suited to address regulatory submissions?”

Today, we’re answering that question with a special edition of Innovit Healthcare Insights – PIM vs PLM Executive Brief.