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Fast Facts

Webinar: 21 CFR Part 11 - Compliance for Electronic Records and Signatures

Regulatory Compliance Training- GlobalCompliancePanel
Mar 24,2010 - Mar 24,2010
Online Webinar, Wilmington, Delaware, United States
 

Highlights

This webinar details the regulation and how it applies to computerized systems. Learn exactly what is needed to be compliant for all three primary areas: SOPs for the IT infrastructure, industry standards for software product features, and the 10-step risk-based validation approach. This webinar demystifies Part 11, and get you on the right track for using electronic records and signatures to greatly increase productivity.

Areas Covered in the Session:

* Which data and systems are subject to Part 11.
* What Part 11 means to you, not just what it says in the regulation.
* Avoid 483 and Warning Letters.
* Explore the three primary areas of Part 11 compliance: SOPs, software product features, and validation documentation.
* Ensure data integrity, security, and protect intellectual property.
* Understand the current computer system industry standards for security, data transfer, and audit trails.
* Electronic signatures, digital pens, and biometric signatures.
* SOPs required for the IT infrastructure.
* Product features to look for when purchasing COTS software.
* Reduce validation resources by using easy to understand fill-in-the-blank validation documents.











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Event Profile

Theme: Regulatory Compliance Training- GlobalCompliancePanel
Sponsors: GlobalCompliancePanel
Speakers: David Nettleton, FDA Compliance Specialist
Attendees: * IT * QA * QC * Laboratory staff * Managers * GMP, GCP, GLP professionals

Contact Details

Contact person: GlobalCompliancePanel
Event website: http://www.globalcompliancepanel.com/control/w_product/~product_id=600139LIVE?channel=mailer&camp=webinar&AdGroup=goingtomeet_MAR24_FEB16
Phone: 800-447-9407
Fax: 302-288-6884

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