Take a closer look at the area where medical devices and pharmaceuticals intersect with this examination of the EU Medical Devices Regulation’s (MDR) first guidance issued on medicinal items which have an “integral medical device” component. The guidance, focused on the implementation of Article 117 of the MDR, is an illustration of how the medical devices and pharmaceuticals industries are increasing their level of collaboration. Find out more about the guidance and the collaborative trend it illustrates in this informative Medtech Insight article.