The most significant change from the MDD to the MDR is the increased focus on clinical evaluation, access to data, and post-market surveillance. This places a greater burden upon manufacturers and their representatives, and it is something that we, at Acorn Regulatory, have been helping our clients with. We have created a brief Clinical Evaluation Report Slide Deck that looks at how you can write an effective clinical evaluation report. This slide deck will give you an overview of the measures that you need to consider when creating a CER for your medical device product.