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

January 6, 2012

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This webinar details all of the templates used to create validation documentation, usually saving two-thirds of the time and costs.

FOR IMMEDIATE RELEASE
(Free-Press-Release.com) January 6, 2012 -- 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

webinars@globalcompliancepanel.com
http://www.globalcompliancepanel.com

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

1000 N West Street | Suite 1200 | Wilmington | DE | Zip 19801 | USA

free-press-release.com computer system validation link requirements online training risk management specificati testing tools

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Contact Information

Name: globalcompliancepanel

Company: GlobalCompliancePanel
Telephone: 8004479407
Email: ***@gmail.com

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