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TZID:America/New_York
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DTSTART:19700308T020000
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UID:2140535:Event:70057
DTSTAMP:20260515T211813Z
SUMMARY:Webinar on Investigating Deviations - Best Practices
DESCRIPTION:Description :\nThis webinar will help attendees understand
  the fundamental steps of a deviation investigation with focus on usin
 g facts and objective evidence to arrive at root cause and CAPA. This 
 webinar will focus on how to avoid the pitfalls that may occur during 
 FDA inspections and help eliminate 483 observations. Learn how to iden
 tify and avoid potential pitfalls during deviation investigations.\nAr
 eas Covered in the Session :\nReview of FDA and Regulatory Requirement
 s for Investigations\nWhat is the definition of a Deviation?\nTypes of
  Deviations/Identification of Deviations\nConducting the Investigation
 \nInterviews – do's and don’ts\nSource Documents/Evidence\nDetermi
 ning Root Cause and Effective/Sustainable CAPA to avoid 483 observatio
 ns\nKey Elements of the Investigation Report\nWho Will Benefit:\nDevia
 tion Investigators\nReviewers and Approvers of Deviation Investigation
 s\nQuality Assurance Departments\nRegulatory Affairs Departments\nQual
 ity Control Departments\nCompliance Auditors\n\nFor more information v
 isit https://medtechiq.ning.com/events/webinar-on-investigating-deviat
 ions-best-practices
DTSTART;TZID=America/New_York:20160616T130000
DTEND;TZID=America/New_York:20160616T140000
CATEGORIES:webinar
LOCATION:Online
WEBSITE:https://compliancetrainings.com/SiteEngine/ProductDetailView.a
 spx?id=FDB1860
URL:https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?
 id=FDB1860
CONTACT:4169154458
ORGANIZER:Compliance Trainings
ATTACH;FMTTYPE="image/jpeg":
ATTENDEE;ROLE=REQ-PARTICIPANT;PARTSTAT=ACCEPTED;RSVP=TRUE;CN=complianc
 etrainings:https://medtechiq.ning.com/profile/compliancetrainings
END:VEVENT
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