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Recent Updates of FDA 21 CFR 11 Add-On Inspections - Conference in Fremont, California, United States on March 2018 by Netzealous LLC DBA - Compliance4All. important dates, call for papers, venue, speakers, abstract submission, research paper, paper submission.
Compliance Trainings & Seminars for all Industries
Both (Technical & Non Technical)
All (State/Province/Region, National & International)
Fremont, California, United States
This presentation will cover the scope, status and results of the
surveillance inspections and what they may mean for the future of 21
CFR Part 11. This will enable you to determine whether your company
is subject to the most common violations so you can take action to
have a better inspection outcome.
Why should you Attend:
In December 2010 the FDA changed the way it does audits to include
21 CFR 11 add-on inspections. Very little is known about this, yet the
FDA has already issued citations on the subject.
Areas Covered In the Session:
What is FDA's most current thinking related to computers and
What are the inspection trends?
What are most frequent recent citations for Part11?
Who Will Benefit:
Everybody using computers in FDA Regulated Environments
IT Manager and Staff
QA Managers and Personnel
Angela Bazigos Seasoned Executive with 40 years of experience in the
Life Sciences & Healthcare Industries. Positions include Chief
Compliance Officer. Experience combines Quality Assurance,
Regulatory Compliance, Business Administration, Information
Technology, Project Management, Clinical Lab Science, Turnarounds
and Business Development.
Event Fee: One Dial-in One Attendee Price: US$150.00