id	author	title	date	pages	extension	mime	words	sentence	flesch	summary	cache	txt
globalce-32	Malataras, Panagiotis; Pallikarakis, Nicolas	Spin-off use of adverse events data: why and how. The case of FDA’s MAUDE	2018	15	.pdf	application/pdf	9959	844	59	However, regarding the EU user reporting system for medical devices adverse events, there is not an overall collection of the reports submitted to the national competent authorities. A significant source of data for medical devices (MDs) appears to come from the medical devices vigilance and post-market surveillance mechanisms that are imposed by the relevant regulatory systems, in most part of the world.	cache/globalce-32.pdf	txt/globalce-32.txt