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Webinar: Internal 21CFR Part 11 Compliance Auditing of Computer Systems
Corporate Compliance Training- GlobalCompliancePanelMar 16,2010 - Mar 16,2010
Wilmington, Delaware, United States
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Highlights
This presentation will describe a proven process for preparing a site for inspection of systems. Case studies will be used to illustrate how this process has successfully prepared several pharmaceutical companies to answer this question accurately, completely and to the great satisfaction of the inspectors. We will review and illustrate audit plans, system inventory, system audits, CAPA and remediation programs.
Why should you attend:
"Show me how you manage your computer systems in compliance with 21CFR Part 11." These words from an FDA or state regulatory inspector can send shivers down your spine. Are you ready for an internal QA or FDA inspection at your site?
Event Reminder
- Registration Open
- Call for Papers
- Call for Speakers
- Receive GTM eblast updates
- Security Code:
Event Profile
- Theme: Corporate Compliance Training- GlobalCompliancePanel
- Sponsors: GlobalCompliancePanel
- Speakers: Richard Poser, President, First Quality Inc
- Attendees: End-users responsible for applications that need to be validated, QA managers and personnel, Information Technology managers and personnel, Validation specialists, Consultants, Quality system auditors , Will provide for
Contact Details
- Contact person: GlobalCompliancePanel
- Event website: http://www.globalcompliancepanel.com/control/w_product/~product_id=600107LIVE/~sel=LIVE?channel=mailer&camp=webinar&AdGroup=GoingToMeet_MAR16_FEB08
- Phone: 800-447-9407
- Fax: 302-288-6884
Tags
- Tag: compliance medical_device iso sox
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