The 2018 MedTech Summit will cover 8 crucial areas: EU MDR, IVDR, Post Market Surveillance and Vigilance, Clinical Evaluations and Investigations for Medical Devices, Medical Device Law, Drug Device Combination Products, Regulatory Affairs in Emerging Markets, and Companion Diagnostics.

AMDR President Dan Vukelich will speak Thursday, June 14th on the European Medical Device Regulation and requirements on the reprocessing of single-use devices. He will also discuss the latest updates on national implementation of reprocessing single-use devices and implications of Common Specifications for industry.