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
- Validation
- IT
- Quality Assurance
- Training
- Manufacturing
Join us for a Webinar on October 27th
Space is limited.
Reserve your Webinar seat now at:
https://www2.gotomeeting.com/register/435619098
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.
System Requirements
PC-based attendees
Required: Windows® 2000, XP Home, XP Pro, 2003 Server, Vista
Macintosh®-based attendees
Required: Mac OS® X 10.4 (Tiger®) or newer
Check out our previous seminars in the Compliance Validation Series
About SyberWorks
SyberWorks, Inc. (www.syberworks.com) is a leader in the custom and Learning Management System industries for Fortune 1000 corporations, higher education, and other industries. Located in Waltham, Massachusetts, the company serves the multi-billion-dollar e-Learning market. Since 1995, SyberWorks has developed and delivered unique and economical solutions to create, manage, measure, and improve e-Learning programs at companies and organizations in the United States, Canada, Europe, and other countries.
About Veracord
Headquartered in San Jose, CA, Veracord (www.veracord.com) serves the FDA regulated life science industry, which includes pharmaceutical, biotechnology, and medical device companies. Veracord offers compliance consulting services nationwide, specializing in validation, IT compliance, clinical, medical, and regulatory affairs. Veracord's signature reflects an uncommon commitment to clients, from handshake to project completion.
Strengthened by its industry experience, including mastery of national and international regulations, Veracord leverages cost-effective, risk-based approaches to validation, with critical-thinking as standard strategy.
Through Veracord's multi-level expertise, clients succeed on several fronts, including across-life-cycle-operations efficiency, cost reduction, and audit-proof compliance. For more information visit: www.veracord.com
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