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VERSION:2.0
PRODID:icalendar-ruby
CALSCALE:GREGORIAN
BEGIN:VEVENT
DTSTAMP:20260819T123801Z
UID:6a56b839-f66b-494c-81f1-0cdbd45fcbc9
DTSTART:20171012T090000Z
DTEND:20171013T170000Z
DESCRIPTION:Things are changing for Medical Devices and IVDs in the Europea
 n Union (EU): new fundamental standards\, new EU device regulations and BR
 EXIT.  What is now needed to enter or\, more importantly\, to maintain pre
 sence in this attractive marketplace for medical devices?  Satisfying requ
 irements harmonized across the 28 member states should be a straightforwar
 d process to get products approved for distribution in each country - but 
 is it?\n\nThis course identifies and explains the requirements – old and
  new – for medical devices\, the steps to obtain entry into the marketpl
 ace (including setting up on-going procedures and relationships)\, the inc
 reasing importance of Clinical Evaluation and Post Market surveillance\, N
 otified Bodies and Competent Authorities.  The course also shares some les
 sons learned from the Course Director\, who has over 25 years of experienc
 e with CE marking medical devices for distribution in the EU.\n
LOCATION:The Berlin Hilton
SUMMARY:Medical Devices: EU Directives\, Guidance\, CE Marking and ISO Stan
 dard Certifications 
URL;VALUE=URI:https://www.cfpie.com/ProductDetails.aspx?ProductID=265
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