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VERSION:2.0
PRODID:icalendar-ruby
CALSCALE:GREGORIAN
BEGIN:VEVENT
DTSTAMP:20260709T145155Z
UID:60c389a3-fa29-488d-aada-6e30b850a380
DTSTART:20171018T090000Z
DTEND:20171020T150000Z
DESCRIPTION:Participants will learn how an effective Process Validation sys
 tem is a critical requirement to the movement toward a risk-based approach
  to compliance and product safety. Also to be discussed is how to tackle p
 rocess validation for medical device combination products.\n\nIssues to be
  covered include:\n•Learn how poor validation procedures and practices c
 an lead to regulatory actions from regulators\n•Assurance of product qua
 lity derived from a compliant validation program\n•Learn how to improve 
 process system knowledge and understanding\n•Learn methods for developin
 g process validations and best practices\n•Understand the scope of regul
 ations governing process validation and identify gaps\n•Develop a plan t
 o rectify existing validation plans\, protocols and reports\n•Learn how 
 to implement and deploy a master validation plan\n
LOCATION:The Berlin Hilton
SUMMARY:Medical Device Validation Training for Professionals
URL;VALUE=URI:https://www.cfpie.com/ProductDetails.aspx?ProductID=261
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