Ten-Step Process for COTS Computer System Validation - Reduce Time and Costs  - Webinar by GlobalCompliancePanel

Ten-Step Process for COTS Computer System Validation - Reduce Time and Costs - Webinar by GlobalCompliancePanel

 

  • General Ticket

    Sale Date Ended

    INR 14674.28
    Sold Out

Invite friends

Contact Us

Page Views : 139

About The Event

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

 

NetZealous LLC,DBA GlobalCompliancePanel 

161 Mission Falls Lane,Suite 216, Fremont, CA 94539, USA           

USA Phone:800-447-9407

Fax: 302-288-6884

webinars@globalcompliancepanel.com

http://www.globalcompliancepanel.com


CLICK HERE