Efficient Computer System Validation - 10 Easy Steps - Webinar By GlobalCompliancePanel
This webinar details all of the templates used to create validation documentation, usually saving two-thirds of the time and costs.
Online, February 8, 2011 (Newswire.com) - 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
Price List:
Live : $245.00
Corporate live : $995.00
Recorded : $295.00
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Tags: Compliance, compliance training, Compliance Webinar, FDA., ISO
