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 |
: | $249 |
: | 416-915-4458 |
: | support@compliancetrainings.com |
: | Compliance Trainings |
: | 4169154458 |
Comments: | None |