UUÂãÁÄÖ±²¥

Phishing warning 01-May-2024
We are aware of phishing emails targeting speakers of events whose names appear on our events pages. If you are unsure if an email regarding event registration or accommodation has come from us please contact us and do not provide any credit card details or personal information.

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

16 March 2011, Wilmington, United States


Introduction
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
Venue
Online Training Webinar

Online Training Webinar, 1000 N West Street | Suite 1200, Wilmington, 19801, United States

Useful links

Organised by
GlobalCompliancePanel
Search
 
 
Showing all upcoming events
Start Date
End Date
Location
Subject area
Event type

Advertisement
Spotlight


E-mail Enquiry
*
*
*
*