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Webinar On Systems Validation Made Easy

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Description: 21 CFR Part 11 provides the basic framework for computer systems used to generate records and data used for analysis and presentation. Validated computerized systems are integral for producing accurate, reliable and consistent data. For many small to mid-sized organizations, proper documentation is a daunting task. In this seminar, we will simplify the validation process and provide practical tips in creating validation documents and procedures that will have you ready for your next audit. We will also provide you with helpful tips when validating commercial off-the-shelf (COTS) software.

Areas Covered in the Session :

Validation Plans, Requirements, Specifications, and Test Reports
Recommended SOPS
Change control
Data backup and business continuity
Tips when validating COTS software
Common audit findings and tips for a successful audit

Who Will Benefit:

This webinar is a must attend for:
Everyone involved in computer system validation
Anyone selecting computer systems intended for FDA regulated environments
Information technology professionals responsible for files or network locations
Quality professionals who organize, document and verify system compliance
Executives evaluating requirements Part 11 compliant systems



URL: https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=IT1212
Date: Thursday, June 12, 2014
Time: 5:00pm-6:00pm UTC
Duration: 1 hour
Access: Public
Created by: Public Access
Updated: Tuesday, April 22, 2014 9:10am UTC
Cost ($): $249
Call In Number: 416-915-4458
Contact Email: support@compliancetrainings.com
Contact Person: Compliance Trainings
Contact Phone: 4169154458
Comments: None



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