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Live Webinar on
Software Validation Planning for Executives and Managers
Date: Wednesday, December 4, 2013 Time: 10:00 AM PST | 01:00 PM EST
Duration: 60 Minutes
Location: Online Register Now
Instructor: David Nettleton
This webinar is intended for executives and managers, and explains the business fundamentals of
regulatory compliance. It explains what does and does not need to be validated. It describes
exactly what is required for compliance with 21 CFR Part 11.
Areas covered in the session:
l What are the fundamentals of regulatory compliance?
l Understand what the regulations mean, not just what they say.
l How to avoid 483 and Warning Letters.
l Which SOPs and validation documents are required?
l Understand the current computer system industry standards for security, data transfer,
audit trails, and electronic signatures.
l How to lower costs, though reduction in resources, and reduction in documentation.
l How to increase productivity by promoting efficient validation and use of computer systems.
Who Will Benefit: About Speaker
l QA FDA Compliance Specialist,
l Managers David is an FDA Compliance Specialist for 21 CFR
l Executives Part 11, HIPAA, and Computer System Validation. His
latest book is "Risk Based Software Validation - Ten
easy Steps" ...more
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