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Webinar On - FDA’s 21 CFR Part 11 Add-on Inspections

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(Free Press Release) Compliance Trainings focuses on providing regulatory and quality web based online trainings to industry professionals across the globe. Compliance Trainings strives to educate and enhance the knowledge and broaden the horizons of regulatory professionals as well as professionals from the HR, Healthcare and many other industries. Regulatory compliance solutions from the house of Compliance Trainings strictly meet international standards and are fundamentally based on the objective of bringing down client compliance costs. Internationally scalable solutions are fully integrated into every webinar or event and help clients meet stringent demands of GxP, ISO and FDA regulatory authorities.

Webinar On - FDA’s 21 CFR Part 11 Add-on Inspections


      

Scheduled On : Thursday, February 27, 2014 at 12:00 Hrs

Description :

In December 2010 the FDA began a project to better understand the industry’s adherence (or lack thereof) to 21 CFR Part 11. This involves the add on’ surveillance inspections of the sponsors’ computer systems during the course of the FDA’s regular inspections.

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. At the beginning of the initiative FDA made it very clear that Part 11 is in effect and is enforced according to the original Part 11 and the Guidance from 2003.

In the meantime FDA officials reported about key findings. For example, George Smith who heads up FDA's Part 11 working group gave an update with examples of violations. This webinar 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.

Areas Covered in the Session :

  • What is FDA's most current thinking related to computers and electronic records?
  • What are the inspection trends?
  • What are most frequent recent citations for Part11?
  • What are the most frequent deviations for computer system validation?
  • Under which circumstances can inspectors exercise enforcement discretion?
  • How important is risk based Part11 compliance?
  • What is the best strategy for future proven Part 11 compliance?

Who Will Benefit:

  • Quality Managers
  • Quality Engineers
  • Small business owners
  • GxP
  • Regulatory Affairs professionals
  • Consultants
  • Quality VPs
  • IT VPs
  • Regulatory VP
  • CEOs

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Webinar On - FDA’s 21 CFR Part 11 Add-on Inspections

Source: Press Release

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