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	Medical device vigilance (Di Renzo Regulatory Affairs) View
	Post Market Surveillance requirements under the new European Medical Device Regulations (GMED North America) View
	Medical Device Reporting (Quality Consultant) View
	SYS-029 Medical Device Reporting (Medical Device Academy) View
	Post-Market Surveillance for medical device industries in the EU: responsibilities and obligations (Profilzentrum Medizintechnik) View
	What is MDR Medical Device Regulation - Introductory Training (Luke Desira) View
	Medical Device Vigilance: Key Insights \| Gaps \| Controversial Terminologies (Healthcare and Regulations: Dr Sarita Ranjan) View
	Interview: Medtronic - Regulatory Affairs Specialist (CTE Foundation Sonoma County) View
	Medical Device Regulation - Regulatory Affairs (Cliniminds India) View
	The European Medical Device New Regulation 2017/745 (WMDO) View