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FDAs 21 CFR 11 AddOn Inspections Recent Updates Webinar by GlobalCompliancePanel

9/10/2013 10:00 AM - 12:00 PM

Overview: In December 2010 FDA started the Part 11 inspection initiative. While originally the initiative was supposed to last 3-6 months, it has now turned into an ongoing program with Part 11 related issues being part of most future inspections.

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 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 you should 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. This Webinar will present the latest on FDA thinking (with slides directly from the FDA's Office of Compliance), discuss how these inspections will impact both your company and the industry, and provide guidance on how your company can ensure that they have a successful inspection.

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?

Who will benefit:

Everybody using computers in FDA Regulated Environments

IT Manager and Staff

QA Managers and Personnel

Regulatory Affairs

Training Departments

Consultants

Validation Specialists

Angela Bazigos, is the CEO of Touchstone Technologies Silicon Valley, Inc. "Your Passport to Compliance". She has 30 years of experience in the Lifesciences industry spanning Project Management, Quality Assurance and Regulatory Affairs and has a patent aimed at speeding up Software Compliance.

NetZealous LLC,

DBA GlobalCompliancePanel

161 Mission Falls Lane,

Suite 216, Fremont, CA 94539, USA

USA Phone:800-447-9407

Fax: 302-288-6884

webinars@globalcompliancepanel.com

http://www.globalcompliancepanel.com

Event Link - http://bit.ly/17mUtn0

Learn More: FDAs 21 CFR 11 AddOn Inspections Recent Updates Webinar by GlobalCompliancePanel

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