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UID:69e509815b96b@leapup.bitshifters.cloud
DTSTAMP:20260419T185737Z
DTSTART:20250521T085500Z
DTEND:20250521T151500Z
SUMMARY:Quality management for medical devices: Introduction and practical implementation
DESCRIPTION:The&nbsp\;quality management system (QMS) of medical device manufacturers&nbsp\;serves as basis for compliance with legal provisions and\, moreover\, enables the organization to produce&nbsp\;safe and reliable products&nbsp\;for the&nbsp\;benefit of patients&nbsp\;and&nbsp\;commercial success. The relevant European legislation&nbsp\;MDR and AI Act&nbsp\;contain concrete requirements that are at least partially fulfilled by the application of the standard&nbsp\;EN ISO 13485.&nbsp\;&nbsp\;\nWhen the&nbsp\;project &ldquo\;Introduction of a quality management system&rdquo\;&nbsp\;starts in an organization\, the question arises of a&nbsp\;suitable roadmap for concrete implementation&nbsp\;with all those involved. In this event\, the realization of the project will be illustrated using a&nbsp\;fictitious model organization. The theoretical basics will be supplemented by&nbsp\;practical examples&nbsp\;from the professional experience of Dr Thorsten Prinz (VDE). The event format offers&nbsp\;sufficient time for your questions and discussions.&nbsp\;\nThe presentations will be given in German. You will receive&nbsp\;all presentation files and example documents as PDF&nbsp\;(in English).&nbsp\;\nWe are looking forward to your participation!&nbsp\;\nMore information here.
LOCATION:MS Teams\, Offenbach am Main
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