This webinar describes a 10-step risk-based approach to validating COTS software in order to reduce costs and documentation requirements by up to two-thirds. Attendees will learn how to link requirements, risk management, and testing to efficiently validate computer systems. The speaker is an industry expert who has completed over 200 validation projects and authored a book on risk-based software validation.

1. Live Webinar on : COTS Software Validation – 10 Easy Steps Monday, April 23, 2012
duration : 01:00 to 02:15 PM EST
Description
This webinar describes efficient techniques for
performing COTS validation. The 10-step risk-based
Get 15 % Discount as an early bird
approach to COTS software validation makes
registration. Use Promo Key :
documentation more manageable and understandable.
CGO15
Learn how to increase productivity and minimize
resources, usually saving two-thirds of the time and
Who will benefit costs. Ensuring compliance of new and upgraded
computer systems. Learn how to use risk management
to improve system performance and promote process
Users of computer systems improvement. After you complete this webinar you
IT will be ready to perform a validation project.
QA
QC
Laboratory staff
Managers Learning Objectives:
Executives
· How to use the risk-based validation
approach to lower costs.
· How to link requirements, specifications, risk
management, and testing.
· Based on: "Risk-Based Software Validation – Ten
Easy Steps" (Davis Horwood International and
PDA - www.pda.org, 2006).

2. purchase formats · Reduce testing by writing test cases that trace to
elements of risk management.
$189 One Dial In - One
Attendee
$249 One Dial In - Unlimited · Learn which documents the FDA expects to
audit.
attendance (To be arranged in a
Conference room/Meeting room.
Note : Only One Dial In Allowed)
· Proven techniques that reduce software costs and
$289 On Demand (Recording implementation times.
available within 48 hrs after the
completion of the webinar)
· Increase corporate productivity and individual
$349 Get Training CD workforce member productivity.
More Trainings · Efficiently create validation documentation.
· Decrease resource requirements.
· Make documentation more manageable and
understandable.
· Avoid 483s and Warning Letters.
· Use resources effectively to perform effective
validation while avoiding doing too much.
- How to implement a computer system to gain
maximum productivity.

3. About Speaker:
Computer System Validation’s principal, David
Nettleton is an industry leader, author, and teacher for
21 CFR Part 11, Annex 11, HIPAA, software validation,
and computer system validation. He is involved with
the development, purchase, installation, operation and
maintenance of computerized systems used in FDA
compliant applications. He has completed more than
206 mission critical laboratory, clinical, and
manufacturing software implementation projects. His
latest book is “Risk Based Software Validation - Ten
easy Steps” (Davis Horwood International and PDA -
www.pda.org, 2006) which provides fill-in-the-blank
templates for completing a COTS software validation
project.
https://compliance2go.com/index.php?option=com_training&speakerkey=19&productKey=81
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