The FDAnews report EU MDR Compliance can help. Our editors have combed through the regulations, picking out the most minute compliance points and building them into a checklist of 200+ requirements you can use to confirm that you are satisfying all the EU mandates for device manufacturing.
A group of sponsors, sites and health IT organizations is working on the first coordinated effort to accelerate and improve the quality of clinical trials through the use of electronic health records and standardized research protocols. The Partnership to Advance Clinical electronic Research, launched last week, hopes to incorporate electronic medical record software into trial-recruitment datasets to provide a clinical network approach to evidence-based drug studies. Clinical Trials Advisor