Efficient Computer System Validation - 10 Easy Steps - Webinar By GlobalCompliancePanel
May 15,2012 - May 15,2012Online 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
Event Reminder
- Registration Open
- Call for Papers
- Call for Speakers
- Receive GTM eblast updates
- Security Code:
Event Profile
- Sponsors: GlobalCompliancePanel
- Speakers: David Nettleton
- Attendees: IT,QA ,QC,Laboratory staff,Managers,GMP, GCP, GLP professionals
Contact Details
Tags
Contact Organizer
