id	author	title	date	pages	extension	mime	words	sentence	flesch	summary	cache	txt
admet-19	Chan, Christopher	On the evaluation of the safety aspects of nanomaterial in medical device – a regulatory perspective	2013	6	.pdf	application/pdf	3135	144	31	3. Risk assessment for nanomaterials For the regulatory control of nano medical devices, in addition to regulations and product pre-market review mechanisms, risk management forms the basis of nano medical device assessment and the establishment of nano medical device regulations. Acknowledgments The Office of Medical Device Evaluation (OMDE) would like to acknowledge the support of the Food and Drug Administration of Taiwan and the Center for Measurement Standards of ITRI towards OMDE’s work in nano medical device risk assessment, and all our team members who made this work feasible.	cache/admet-19.pdf	txt/admet-19.txt