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DTSTAMP:20260718T231343Z
UID:1ccd55ca-637f-4a17-81f9-97f86bf7d935
DTSTART:20171016T090000Z
DTEND:20171017T170000Z
DESCRIPTION:The regulatory and business requirements for the pharma\, diagn
 ostics\, and medical-device fields continue to update\, blend\, overlap\, 
 and blur. With these changes\, the importance of risk assessment—and ris
 k management—gains higher business and regulatory significance. It now b
 ecomes even more important for professionals in these fields to recognize\
 , accept\, understand\, and respond to these changes —particularly since
  new regulatory requirements have emerged within this changing environment
 .\n\nThe market’s Tolerance for Failure of Drugs\, Devices\, and IVDs ha
 s reduced significantly in recent decades. This reduction reflects a gener
 al loss of confidence in the medical industry. The adoption of formal Qual
 ity Management Systems (QMS) has recovered some of that confidence\, but w
 e must still do more. This course addresses what we can do.\n
LOCATION:The Berlin Hilton
SUMMARY:Integration of Risk Management Principles and Activities into the Q
 uality System
URL;VALUE=URI:https://www.cfpie.com/Custom/Catalog.aspx?C=22&L=4&D=0
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