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very good morning everyone welcome to global compliance panels live webinar on design history file device master record device history record and technical file regulatory documents explained my name is Nathan and Im going to be your host today on behalf of the global compliance panel team I would like to thank you for being part of this event todays webinar will be presented by mr. Jeff Nassif mr. Jeff get off is the director of quality at meditators a leading manufacturer of endoscopy and colonoscopy devices where he oversees the operation of the quality system in this position Jeff is responsible for oversight of the document control system including maintenance of regulatory documentation right with this Jeff spent 13 years at life tech as the director of regulatory affairs where he was responsible for compliance of the corporate quality system just received his regulatory of their affair certification in 1996 we are honored to have such a distinguished person such as Jeff Cassa