FDA Compliance 2012 - FDA's new enforcement initiative ? Strategic Software Validation Planning for Executives and Managers
Date2012-01-12
Deadline2012-01-12
VenuePalo Alto, USA - United States
KeywordsSoftware validation compliance, FDA enforcement initiative, FDA software validation regulatory requirements, 21 CFR Part 11 compliance training
Topics/Call fo Papers
This Software Validation training webinar will discuss how to approach Strategic software Validation planning so as to satisfy FDA by complying to new enforcement initiative by FDA.
Why should you Attend:
FDA Commissioner Margaret Hamburg recently announced several new enforcement initiatives. They are certain to impact your regulatory risk profile. How will you prepare for software quality, software validation and 21 CFR part 11 planning?
Extensive use of automated manufacturing, laboratory, QA, QC, complaints, CAPA, Adverse Events systems puts companies at risk. FDA field staff has been trained on software validation and 21 CFR Part 11 inspection and enforcement. Many companies have fallen behind in their software validation practices. Now is the time for forward planning in this crucial area. This executive planning session discusses the key elements on which to focus. The attendee should leave this strategic planning session confident in knowing how FDA will approach software validation enforcement and how to prevent needless inspections, as well as how to satisfy an FDA inspector.
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Last modified: 2011-10-04 15:16:10