2012 - Efficient Computer System Validation - 10 Easy Steps - Webinar By GlobalCompliancePanel

Overview: This webinar details all of the templates used to create validation documentation, usually saving two-thirds of the time and costs. The 10-step risk-based approach to COTS software validation minimized documentation and ensures efficient implementation of new and upgraded computer systems. This experience will prepare you to perform a validation project.

Areas Covered in the Session:
Learn which documents the FDA expects to audit.
How to use the risk-based validation approach to lower costs.
How to link requirements, specifications, risk management, and testing.
Document a computer system validation project using easy to understand fill-in-the-blank templates.
Based on: "Risk-Based Software Validation ? Ten Easy Steps" (Davis Horwood International and PDA - www.pda.org, 2006).
Step-by-step instructions for performing and documenting a risk assessment, and how to use the results to reduce validation documentation.
Reduce testing by writing test cases that trace to elements of risk management.
Who Will Benefit:
IT
QA
QC
Laboratory staff
Managers
GMP, GCP, GLP professionals

Tuesday, May 15, 2012
10:00 AM PDT | 01:00 PM EDT

Price List:
Live : $245.00
Corporate live : $995.00
Recorded : $295.00

webinars-AT-globalcompliancepanel.com
http://www.globalcompliancepanel.com

Phone: 800-447-9407
Fax: 302-288-6884