Conference Description:
Understand 10 step Risk based approach to validation, explore methods to decrease resource requirements and make documentation more manageable and understandable.
Areas Covered in the Seminar:
. Learn which documents the FDA expects to audit.
. Proven techniques that reduce software costs and implementation times.
. Increase corporate productivity and individual workforce member productivity.
. Efficiently create validation documentation.
. Decrease resource requirements.
. Make documentation more manageable and understandable.
. Avoid 483s and Warning Letters.
. How to implement a computer system to gain maximum productivity.
. Use resources effectively to perform effective validation while avoiding doing too much.
. 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).
For More Details:
http://www.complianceonline.com/ecomme rce/control/trainingFocus/~product_id=70 1583?channel=worldconf
Start Date: 2010-08-05
Last Day: 2010-08-05
Contact Person: admin
Email: admin@complianceonline.com
Address:
2600 E. Bayshore Road, Palo Alto, CA, 94303, United States
Tel: 650-620-3915
Fax: 650-963-2556
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