Webinar: 21 CFR Part 11 - Compliance for Electronic Records and Signatures
Regulatory Compliance Training- GlobalCompliancePanelMar 24,2010 - Mar 24,2010
Online Webinar, Wilmington, Delaware, United States
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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.

Event Reminder
- Registration Open
- Call for Papers
- Call for Speakers
- Receive GTM eblast updates
- Security Code:
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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