Medical Devices - Impacts of MDR in EU - By Deloitte
This paper looks to understand the range of impacts the EU MDR will have on the industry—from change management to portfolio reviews to product labelling. Deloitte propose a series of steps manufacturers should take to address and mitigate the changes ahead. With careful planning, a successful transition to the new regulatory landscape is possible. Link: https://www2.deloitte.com/content/dam/Deloitte/global/Documents/Life-Sciences-Health-Care/gx-eu-med-device-regulation.pdf