21 CFR Part 11 and Its Application in a Compliant Environment
Who should attend?
Professionals who work in the healthcare, pharmaceutical, life science, biotechnology, medical-manufacturing, medical device, and other highly regulated industries in the following areas:
- FDA/GxP/GAMP Compliance
- Quality Assurance
Space is limited.
Reserve your Webinar seat now at:
In August 1997, the FDA published the rules for electronic signatures and electronic records entitled 21 CFR Part 11: Electronic Signatures, Electronic Records. This Webinar discusses the history behind 21 CFR Part 11, correlation between 21 CFR Part 11 and other CFRs, and the general concepts of security in a Part 11 compliant system.
Title:21 CFR Part 11 and Its Application in a Compliant Environment
Date: Tuesday, October 27, 2009
Time:2:00 PM - 3:00 PM EST; 1:00 PM - 2:00 PM CST; Noon - 1:00 PM MST; 11:00 AM - Noon PST
After registering you will receive a confirmation email containing information about joining the Webinar.
Required: Windows® 2000, XP Home, XP Pro, 2003 Server, Vista
Required: Mac OS® X 10.4 (Tiger®) or newer
Check out our previous seminars in the Compliance Validation Series
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