How Natural Language Processing Improves Clinical Evaluation Reports for Medical Devices
The EU Medical Device Regulation (MDR) of 2017 (also known as Regulation (EU) 2017/745) has had a huge impact on the regulation of medical devices in Europe, including more stringent manufacturer oversight and increased post-market surveillance. Although medical devices approved prior to Regulation (EU) 2017/745 coming into force had been granted a three-year transitionary period,…