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UID:2140535:Event:115965
DTSTAMP:20260526T131609Z
SUMMARY:Updated CE Marking Process & ISO 13485:2016 Expectations
DESCRIPTION:Overview:After completion of this course, attendees will h
 ave enhanced knowledge of the ever-changing landscape of Medical Devic
 e Regulation in the EU.\nLearning Objective:\nUpon completion of this 
 course, attendees will have enhanced knowledge of the ever-changing la
 ndscape of Medical Device Regulation in the EU.\nThe content of this c
 ourse is designed to simplify the understanding of requirements and to
  provide attendees with the latest insight on how changes are being vi
 ewed and implemented by companies marketing products in the EU.\nWho W
 ill Benefit:Quality AssuranceRegulatory AffairsClinical Research and M
 edical OperationsProduct Development\nSpeaker Profile:\nEvent Fee: One
  Dial-in One Attendee Price: US $150.00\nContact Detail:Compliance4All
  DBA NetZealous,Phone: +1-800-447-9407Email: compliance4all14@gmail.co
 m\n\nFor more information visit https://medtechiq.ning.com/events/upda
 ted-ce-marking-process-amp-iso-13485-2016-expectations-1
DTSTART;TZID=America/New_York:20190712T100000
DTEND;TZID=America/New_York:20190712T113000
CATEGORIES:webinar
LOCATION:Online
WEBSITE:https://www.compliance4all.com/control/w_product/~product_id=5
 02567LIVE?channel=medtechiq_Jul_2019_SEO
URL:https://www.compliance4all.com/control/w_product/~product_id=50256
 7LIVE?channel=medtechiq_Jul_2019_SEO
CONTACT:18004479407
ORGANIZER;CN="Adam Fleming":https://medtechiq.ning.com/profile/Complia
 nce4all
ATTACH;FMTTYPE="image/jpeg":https://storage.ning.com/topology/rest/1.0
 /file/get/2647295700?profile=original
ATTENDEE;ROLE=REQ-PARTICIPANT;PARTSTAT=ACCEPTED;RSVP=TRUE;CN="Adam Fle
 ming":https://medtechiq.ning.com/profile/Compliance4all
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