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Fast Facts

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

May 15,2012 - May 15,2012
Online Training, Washington, Delaware, United States
 

Highlights

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 : $245.00Corporate live : $995.00Recorded : $295.00
webinars@globalcompliancepanel.com http://www.globalcompliancepanel.com
Phone: 800-447-9407Fax: 302-288-6884











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Event Profile

Sponsors: GlobalCompliancePanel
Speakers: David Nettleton
Attendees: IT,QA ,QC,Laboratory staff,Managers,GMP, GCP, GLP professionals

Contact Details

Contact person: webinars
Event website: http://bit.ly/HCMcl5
Phone: 800-447-9407
Fax: 302-288-6884

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